ClearanceBrief
510(k) K220875 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

HAcancellous PEEK-C Porous HA PEEK Cervical IBF System

ApplicantInnovasis, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Aug 26, 2022
ReceivedMar 25, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220875

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.