K012923 is an FDA 510(k) clearance for the ARTHREX FIBERWIRE, USP SIZE 5, MODEL AR-7201. This device is classified as a Suture, Nonabsorbable, Synthetic, Polyethylene (Class II - Special Controls, product code GAT).
Submitted by Arthrex, Inc. (Naples, US). The FDA issued a Cleared decision on October 4, 2001, 34 days after receiving the submission on August 31, 2001.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.5000.
| 510(k) Number | K012923 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 31, 2001 |
| Decision Date | October 04, 2001 |
| Days to Decision | 34 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 |