510(k) K241008 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Tricera Arthroscopic System; Tricera Controller (R-10001); Tricera Handpiece, Autoclavable (R-10023); Veriflow (R-10003); Exoflow (R-10017); 3-in-1 Shaver 4.2mm (R-10008); 3-in-1 Shaver 5.0mm (R-10014); Dynablator (R-10005); Standard Burr 5.0mm (R-10021); Standard Shaver 3.4mm (R-10012); Curved Sta
| Applicant | Relign Corporation, Subsidiary of Zimmer Biomet, Campbell CA, US |
| Decision | Substantially Equivalent, May 8, 2024 |
| Received | Apr 12, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K241008
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.