ClearanceBrief
510(k) K222903 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

Tailored-H Cervical Stand Alone System

ApplicantBespoke Technologies, LLC, Winston-Salemn NC, US
DecisionSubstantially Equivalent, Nov 18, 2022
ReceivedSep 23, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222903

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.