510(k) K780225 ยท IQI Orthosis, Limb Brace
ORTHOSISES DEVICES
| Applicant | Biomet, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 24, 1978 |
| Received | Feb 9, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780225
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.