K111695 is an FDA 510(k) clearance for the HYBRID GRAFT. This device is classified as a Mesh, Surgical, Polymeric (Class II - Special Controls, product code FTL).
Submitted by Cook Biotech, Inc. (West Lafayette, US). The FDA issued a Cleared decision on April 2, 2012, 291 days after receiving the submission on June 16, 2011.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3300.
| 510(k) Number | K111695 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 16, 2011 |
| Decision Date | April 02, 2012 |
| Days to Decision | 291 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FTL — Mesh, Surgical, Polymeric |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3300 |