510(k) K902332 ยท HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
HALL MODULAR ACETABULAR REAMER SYSTEM
| Applicant | Zimmer, Inc., Carpinteria CA, US |
| Decision | Substantially Equivalent, Jun 25, 1990 |
| Received | May 24, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902332
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.