510(k) K030388 ยท HWC Screw, Fixation, Bone
IMPACT SUTURE ANCHOR. MODEL 433510
| Applicant | Bionx Implants, Ltd., Tampere, FI |
| Decision | Substantially Equivalent, Apr 24, 2003 |
| Received | Feb 5, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030388
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.