510(k) K132217 ยท HWC Screw, Fixation, Bone
ARTHREX COMPRESSION FT SCREWS
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Nov 25, 2013 |
| Received | Jul 17, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132217
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.