510(k) K072848 ยท HWC Screw, Fixation, Bone
ACTIVASCREW
| Applicant | Bioretec, Ltd., Tampere, FI |
| Decision | Substantially Equivalent, Nov 2, 2007 |
| Received | Oct 4, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072848
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.