K962971 is an FDA 510(k) clearance for the POLYPROPYLENE MESH (VARIOUS SIZES). This device is classified as a Mesh, Surgical, Polymeric (Class II - Special Controls, product code FTL).
Submitted by Davis & Geck, Inc. (St. Louis, US). The FDA issued a Cleared decision on September 16, 1996, 47 days after receiving the submission on July 31, 1996.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3300.
| 510(k) Number | K962971 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 31, 1996 |
| Decision Date | September 16, 1996 |
| Days to Decision | 47 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Statement |
| Product Code | FTL — Mesh, Surgical, Polymeric |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3300 |