510(k) K081893 ยท HWC Screw, Fixation, Bone
OPUS MAGNUM SPEEDSCREW KNOTLESS FIXATION DEVICE, MODEL OM-6500
| Applicant | Arthrocare Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 1, 2008 |
| Received | Jul 3, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081893
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.