510(k) K052607 ยท HWC Screw, Fixation, Bone
ARTHREX INTERFERENCE SCREW-ROUNDED HEAD SCREWS, FULL THREADED SCREWS, SHEATHED CANNULATED INTERFERENCE SCREWS
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Nov 7, 2005 |
| Received | Sep 22, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052607
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.