510(k) K250752 · GWG Endoscope, Neurological
AURORA® Surgiscope® System (ASX15/60); AURORA® Surgiscope® System (ASX15/80)
| Applicant | Integra LifeSciences Corporation, Princeton NJ, US |
| Decision | Substantially Equivalent, Apr 9, 2025 |
| Received | Mar 12, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K250752
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.