510(k) K003816 ยท HWC Screw, Fixation, Bone
ARTHREX TITANIUM CORKSCREW, 3.5 MM, ARTHREX TITANIUM CORKSCREW, 5.0 MM, ARTHREX TITANIUM CORKSCREW 6.5MM
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Mar 9, 2001 |
| Received | Dec 11, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003816
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.