510(k) K951263 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
INTRAARC DRIVE SYSTEM
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Apr 17, 1995 |
| Received | Mar 21, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951263
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.