510(k) K010884 ยท HWC Screw, Fixation, Bone
TITANIUM COMPRESSION ANCHOR SYSTEM
| Applicant | Anchor Medical Technologies, Irvine CA, US |
| Decision | Substantially Equivalent, Jun 20, 2001 |
| Received | Mar 23, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010884
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.