510(k) K022234 ยท HWC Screw, Fixation, Bone
ARTHREX WRIST BIO-ANCHOR, MODEL AR-1322B
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Oct 3, 2002 |
| Received | Jul 11, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022234
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.