510(k) K010525 ยท HWC Screw, Fixation, Bone
ARTHREX TENODESIS SCREW 7MM, 8MM, 9MM
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, May 23, 2001 |
| Received | Feb 22, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010525
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.