510(k) K050766 ยท HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
EXPLANT OSTEONECROSIS INTERVENTION IMPLANT REMOVAL SYSTEM
| Applicant | Zimmer Trabecular, Allendale NJ, US |
| Decision | Substantially Equivalent, May 26, 2005 |
| Received | Mar 25, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050766
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.