MINI TIGHTROPE — Arthrex, Inc. (510(k) K090107)
MINI TIGHTROPE — Arthrex, Inc. (510(k) K090107) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: MINI TIGHTROPE; Applicant: Arthrex, Inc.; Clearance track: 510(k).
| Device name | MINI TIGHTROPE |
|---|---|
| Applicant | Arthrex, Inc. |
| Clearance track | 510(k) |
| Submission number | K090107 |
| Decision | Substantially Equivalent |
| Decision date | 2009-08-06 |
| Date received | 2009-01-15 |
| Product code | HTN |
| Device class | 2 |
| Medical specialty | Orthopedic |
| Applicant location | FL, US |
| Source | openFDA device |
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$1999/mo
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