510(k) K250417 ยท QSM System, Surgical, Computer Controlled Instrument, Remanufactured
Remanufactured EndoWrist Cobra Grasper (420190)
| Applicant | Rebotix, St. Petersburg FL, US |
| Decision | Substantially Equivalent, Aug 20, 2025 |
| Received | Feb 13, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250417
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.