K053631 is an FDA 510(k) clearance for the CONTOUR TRANSTAR CURVED CUTTER STAPLER SET, a Staple, Implantable (Class II — Special Controls, product code GDW), submitted by Ethicon Endo-Surgery, Inc. (Cincinnati, US). The FDA issued a Cleared decision on January 30, 2006, 32 days after receiving the submission on December 29, 2005. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4750.
| 510(k) Number | K053631 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | December 29, 2005 |
| Decision Date | January 30, 2006 |
| Days to Decision | 32 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | GDW — Staple, Implantable |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.4750 |