510(k) K880413 ยท LXH Orthopedic Manual Surgical Instrument
PATELLAR TENDON GRAFT GUIDE
| Applicant | Concept, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Mar 4, 1988 |
| Received | Feb 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880413
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.