510(k) K930125 ยท HXA Prosthesis, Tendon, Passive
PHOENIX BONE SCREWS PBS-TYPE SERIES
| Applicant | Phoenix Bioengineering, Inc., Bridgeport PA, US |
| Decision | Substantially Equivalent, Dec 30, 1993 |
| Received | Jan 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930125
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.