510(k) K051726 ยท HWC Screw, Fixation, Bone
ARTHREX TENODESIS FAMILY
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Sep 27, 2005 |
| Received | Jun 28, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051726
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.