ClearanceBrief
510(k) K231899 · ODP Intervertebral Fusion Device With Bone Graft, Cervical

HAtetracell™-C Titanium Cervical IBF System

ApplicantInnovasis, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Oct 17, 2023
ReceivedJun 28, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231899

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.