ClearanceBrief
510(k) K223510 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

Matrix HA Fusion Porous Cervical IBF System

ApplicantInnovasis, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Dec 12, 2022
ReceivedNov 22, 2022
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K223510

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.