510(k) K024086 ยท HWC Screw, Fixation, Bone
PROPELLER HEAD SMALL CANNULATED SCREW SYSTEM
| Applicant | Biomet Orthopedics, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jan 9, 2003 |
| Received | Dec 11, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K024086
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.