510(k) K885229 ยท HSZ Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/Attachment
MODIFIED GLENOID ARCUATE DRILL & DISP. FLEXI-BITS
| Applicant | Romano Surgical Instrumentation, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Sep 29, 1989 |
| Received | Dec 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885229
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.