510(k) K102802 ยท GYC Electrode, Cortical
INTEGRA ELECTRODE TUNNELING NEEDLE
| Applicant | Integra LifeSciences Corporation, Planisboro NJ, US |
| Decision | Substantially Equivalent, Nov 23, 2010 |
| Received | Sep 27, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102802
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.