ClearanceBrief
510(k) K142744 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

Mecta-C TiPEEK

ApplicantMedacta International, Castel San Pietro, CH
DecisionSubstantially Equivalent, May 7, 2015
ReceivedSep 24, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142744

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.