ClearanceBrief
510(k) K212266 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

FIX-C PEEK Anterior Cervical Interbody System

ApplicantJeil Medical Corporation, Seoul, KR
DecisionSubstantially Equivalent, Dec 21, 2021
ReceivedJul 20, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K212266

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.