K102339 is an FDA 510(k) clearance for the CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE, a Suture, Nonabsorbable, Synthetic, Polyethylene (Class II — Special Controls, product code GAT), submitted by Conmed Linvatec (Largo, US). The FDA issued a Cleared decision on November 23, 2010, 97 days after receiving the submission on August 18, 2010. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.5000.
| 510(k) Number | K102339 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 18, 2010 |
| Decision Date | November 23, 2010 |
| Days to Decision | 97 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | GAT — Suture, Nonabsorbable, Synthetic, Polyethylene |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.5000 |