K030782 is an FDA 510(k) clearance for the SEAMGUARD BIOABSORBABLE STAPLE LINE REINFORCEMENT MATERIAL. This device is classified as a Mesh, Surgical (Class II - Special Controls, product code FTM).
Submitted by W.L. Gore & Associates, Inc. (Flagstaff, US). The FDA issued a Cleared decision on April 21, 2003, 41 days after receiving the submission on March 11, 2003.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3300.
| 510(k) Number | K030782 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 11, 2003 |
| Decision Date | April 21, 2003 |
| Days to Decision | 41 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 |