510(k) K960852 ยท HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
HALL MODULAR ACETABULAR REAMER SYSTEM
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Mar 20, 1996 |
| Received | Mar 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960852
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.