ClearanceBrief
510(k) K160605 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

MectaLIF Anterior Stand-Alone

ApplicantMedacta International, Castel San Pietro, CH
DecisionSubstantially Equivalent, Jul 21, 2016
ReceivedMar 2, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160605

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.