510(k) K963432 ยท LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
GUIDE WIRES FOR CANNULATED SCREWS
| Applicant | Orthopaedic Biosystems, Ltd., Scotsdale AZ, US |
| Decision | Substantially Equivalent, Nov 13, 1996 |
| Received | Aug 30, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963432
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.