510(k) K053543 ยท HWC Screw, Fixation, Bone
ARTHREX ARTHOERESIS IMPLANT
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Apr 3, 2006 |
| Received | Dec 20, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053543
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.