K120605 is an FDA 510(k) clearance for the PERMACOL SURGICAL IMPLANT. This device is classified as a Mesh, Surgical (Class II - Special Controls, product code FTM).
Submitted by Covidien, LLC (Bedford, US). The FDA issued a Cleared decision on May 18, 2012, 80 days after receiving the submission on February 28, 2012.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3300.
| 510(k) Number | K120605 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 28, 2012 |
| Decision Date | May 18, 2012 |
| Days to Decision | 80 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FTM — Mesh, Surgical |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3300 |