510(k) K062980 ยท HWC Screw, Fixation, Bone
ACTIVASCREW
| Applicant | Bioretec, Ltd., Tampere, FI |
| Decision | Substantially Equivalent, Nov 22, 2006 |
| Received | Sep 29, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062980
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.