510(k) K241872 ยท QSM System, Surgical, Computer Controlled Instrument, Remanufactured
Remanufactured EndoWrist ProGrasp Forceps (420093)
| Applicant | Rebotix, St. Petersburg FL, US |
| Decision | Substantially Equivalent, Nov 7, 2024 |
| Received | Jun 27, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241872
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.