ARTHREX FIBERTAPE (TM), 2MM, ARTHREX FIBERTAPE (TM), 3MM, ARTHREX FIBERTAPE (TM), 4MM, MOD — Arthrex, Inc. (510(k) K032245)
ARTHREX FIBERTAPE (TM), 2MM, ARTHREX FIBERTAPE (TM), 3MM, ARTHREX FIBERTAPE (TM), 4MM, MOD — Arthrex, Inc. (510(k) K032245) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: ARTHREX FIBERTAPE (TM), 2MM, ARTHREX FIBERTAPE (TM), 3MM, ARTHREX FIBERTAPE (TM), 4MM, MOD; Applicant: Arth
| Device name | ARTHREX FIBERTAPE (TM), 2MM, ARTHREX FIBERTAPE (TM), 3MM, ARTHREX FIBERTAPE (TM), 4MM, MOD |
|---|---|
| Applicant | Arthrex, Inc. |
| Clearance track | 510(k) |
| Submission number | K032245 |
| Decision | Unknown |
| Decision date | 2004-01-14 |
| Date received | 2003-07-22 |
| Product code | GAT |
| Device class | 2 |
| Medical specialty | General, Plastic Surgery |
| Applicant location | FL, US |
| Source | openFDA device |
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