Ex Parte HartleyDownload PDFPatent Trial and Appeal BoardMar 19, 201310962766 (P.T.A.B. Mar. 19, 2013) Copy Citation UNITED STATES PATENT AND TRADEMARKOFFICE UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O. Box 1450 Alexandria, Virginia 22313-1450 www.uspto.gov APPLICATION NO. FILING DATE FIRST NAMED INVENTOR ATTORNEY DOCKET NO. CONFIRMATION NO. 10/962,766 10/12/2004 INV001David Ernest Hartley 12730-635 (PA-5368-RFB) 8509 48003 7590 03/19/2013 BRINKS HOFER GILSON & LIONE/CHICAGO/COOK PO BOX 10395 CHICAGO, IL 60610 EXAMINER SZPIRA, JULIE ANN ART UNIT PAPER NUMBER 3731 MAIL DATE DELIVERY MODE 03/19/2013 PAPER Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE __________ BEFORE THE PATENT TRIAL AND APPEAL BOARD __________ Ex parte DAVID ERNEST HARTLEY __________ Appeal 2011-006990 Application 10/962,766 Technology Center 3700 __________ Before DEMETRA J. MILLS, JEFFREY N. FREDMAN, and JOHN G. NEW, Administrative Patent Judges. FREDMAN, Administrative Patent Judge. DECISION ON APPEAL This is an appeal under 35 U.S.C. § 134 involving claims to a stent graft. The Examiner rejected the claims as anticipated and as obvious. We have jurisdiction under 35 U.S.C. § 6(b). We reverse. Appeal 2011-006990 Application 10/962,766 2 Statement of the Case Background “This invention relates to a stent graft for use in the human or animal body and more particularly to a stent graft which can be used as a side branch stent graft from a main vessel stent graft” (Spec. 1, ll. 6-8). The Claims Claims 3-6 and 24 are on appeal. Claim 24 is representative and reads as follows: 24. A stent graft comprising a tubular body of a biocompatible graft material, the tubular body comprising a first end and a second end, a lumen therethrough, being of a selected diameter and the tubular body comprising an inside and an outside, a balloon radially expandable stent inside the first end of the tubular body and an extension portion of the balloon radially expandable stent extending longitudinally beyond the first end of the tubular body whereby the extension portion of the balloon expandable stent can be expanded with a balloon to expand radially beyond the selected diameter of the tubular body, a plurality of self radially expanding stents spaced apart on the tubular body and positioned on the outside of the tubular body towards the second end of the tubular body and a terminal self radially expanding stent on the inside of the tubular body at the second end of the tubular body. The issues A. The Examiner rejected claims 3-5 and 24 under 35 U.S.C. § 102(e) as anticipated by Greenberg1 (Ans. 3-4). B. The Examiner rejected claim 6 under 35 U.S.C. § 103(a) as obvious over Greenberg (Ans. 5). 1 Greenberg, et al., US 2002/0198587 A1, published Dec. 26, 2002. Appeal 2011-006990 Application 10/962,766 3 A. 35 U.S.C. § 102(e) over Greenberg The Examiner finds that Greenberg teaches: a stent graft comprising a tubular body of a biocompatible material . . . comprising a first end and a second end, a lumen . . . of a selected diameter and . . . a balloon radially expandable stent . . . and an extension portion of the balloon radially expandable stent extending longitudinally beyond the first end of the tubular body whereby the extension portion of the balloon radially expandable stent can be expanded with a balloon (paragraph 49) to expand radially beyond the selected diameter of the tubular body and a plurality of self radially expanding stent . . . spaced apart on the tubular body and positioned on the outside of the tubular body and a terminal self radially expanding stent (58) on the inside of the tubular body. (Ans. 3-4). Appellant contends that “Greenberg does not disclose a balloon expandable stent positioned in inside a tubular body at one end of the tubular” (App. Br. 10). Appellant contends that Greenberg “does not disclose that balloon expandable stent resides inside a tubular body with a portion that extends beyond the end of the tubular body . . . the attachment stent 32 is attached to the very end of the device and is not inside as recited by claim 24” (App. Br. 12). The issue with respect to this rejection is: Does the evidence of record support the Examiner’s conclusion that Greenberg anticipates claim 24? Findings of Fact 1. Greenberg teaches that “the stent graft assembly 10 is modular and comprises an aortic section or a aortic section 12, an iliac section 14, and a contralateral iliac occluder 80” (Greenberg 2 ¶ 0026). Appeal 2011-006990 Application 10/962,766 4 2. Figure 1 of Greenberg is reproduced below: “FIG. 1 diagrammatically illustrates the stent graft assembly of the present invention deployed within a ruptured aneurysm, and an occluder in a selected iliac artery” (Greenberg 2 ¶ 0015). Appeal 2011-006990 Application 10/962,766 5 3. Greenberg teaches that: The aortic section 12 includes a proximal end portion 26 . . . An attachment stent 32 is secured to the proximal end portion, with the stent’s distal end portion 34 along the inside surface of the graft material 36, while the remaining attachment portion 38 extending proximally from the graft material and having barbs 40 for example for becoming affixed to the vessel walls. (Greenberg 2-3 ¶ 0028). 4. Greenberg teaches that “[o]ptionally, a molding balloon may be used to inflate within self-expanded attachment stent 32 to assuredly press the struts against the vessel wall and seat the barbs” (Greenberg 5 ¶ 0049). 5. Greenberg teaches that the “stents are preferably well-known self-expanding Gianturco Z-stents, however, balloon expandable stents an also be used” (Greenberg 6 ¶ 0055). 6. Figure 13 of Greenberg is reproduced below: “FIG. 13 illustrates attachment stent 32 before top cap 104 has been placed over the exposed struts 148” (Greenberg 5 ¶ 0048). Appeal 2011-006990 Application 10/962,766 6 Principles of Law “A single prior art reference that discloses, either expressly or inherently, each limitation of a claim invalidates that claim by anticipation.” Perricone v. Medicis Pharmaceutical Corp., 432 F.3d 1368, 1375 (Fed. Cir. 2005). Analysis Greenberg teaches a modular stent graft with tubular bodies (FF 1) which comprise self-expanded stents (FF 2-3). We agree with Appellant that “the use of a molding balloon on a self-expanding stent after it has been expanded is not the same as using a balloon expandable stent” (App. Br. 11). The structure of self-expanding and balloon stents are different, and even if a balloon is later used to mold the self-expanding stent, it maintains a different structure than a balloon expanding stent. Further, Greenberg does not teach the combination of balloon expandable stents and radially expandable stents spaced apart on the tubular body. We recognize that Greenberg suggests that balloon expandable stents and self-expanding stents are known equivalents (FF 5). However, the current rejection is not an obviousness rejection under 35 U.S.C. § 103(a) where we can rely upon known equivalence to support a finding of prima facie obviousness. Instead, the current rejection is an anticipation rejection. As stated in Arkley, an anticipatory reference under 35 U.S.C. § 102 [M]ust clearly and unequivocally disclose the claimed compound or direct those skilled in the art to the compound without any need for picking, choosing, and combining various disclosures not directly related to each other by the teachings of the cited reference. Such picking and choosing may be entirely proper in the making of a 103, obviousness Appeal 2011-006990 Application 10/962,766 7 rejection, where the applicant must be afforded an opportunity to rebut with objective evidence any inference of obviousness which may arise from the similarity of the subject matter which he claims to the prior art, but it has no place in the making of a 102, anticipation rejection. In re Arkley, 455 F.2d 586, 587-588 (CCPA 1972). The instant situation is similar to Arkley, where affirmance of the rejection would require picking and choosing from the reference in order to arrive at the claimed invention. That is, to satisfy claim 24, we would need to replace the self-expanding stent at the end of the tubular body taught by Greenberg with a balloon expandable stent, but retain the remaining self- expanding stents spaced apart on the tubular body. We do not address whether this would have been obvious, since that question is not presented. We simply find that claim 24 is not anticipated. Conclusion of Law The evidence of record does not support the Examiner’s conclusion that Greenberg anticipates claim 24. B. 35 U.S.C. § 103(a) over Greenberg The Examiner finds that it “is well known in the art that stents can be made from a nickel, titanium or magnesium alloy” (Ans. 5). The Examiner also finds it obvious to “use a shape memory alloy” (Ans. 5). We agree with Appellant that “the Examiner provides no evidentiary support for the conclusory statement in the Final Office Action” (App. Br. 15). In this case, Appellant traverse the Examiner’s finding. When the Examiner is challenged as to what was well known, the Examiner is required Appeal 2011-006990 Application 10/962,766 8 to produce objective evidence which supports the fact(s) at issue. The Examiner has failed in this burden in the instant case to provide any such evidence. See In re Ahlert, 424 F.2d 1088, 1091 (CCPA 1970) (“Assertions of technical facts in areas of esoteric technology must always be supported by citation to some reference work recognized as standard in the pertinent art and the appellant given, in the Patent Office, the opportunity to challenge the correctness of the assertion or the notoriety or repute of the cited reference”). We do not specifically address whether stents made of shape memory materials such as nitinol are well known in the art, because the Examiner has failed to establish a prima facie case by failing to provide evidence supporting this fact. It is not the role of the Board to properly formulate a rejection which has been inadequately articulated. SUMMARY In summary, we reverse the rejection of claims 3-5 and 24 under 35 U.S.C. § 102(e) as anticipated by Greenberg. We reverse the rejection of claim 6 under 35 U.S.C. § 103(a) as obvious over Greenberg REVERSED dm Copy with citationCopy as parenthetical citation