ClearanceBrief
510(k) K072465 ยท MQP Spinal Vertebral Body Replacement Device

NIKO CORPECTOMY SPACER

ApplicantGlobus Medical, Inc., Audubon PA, US
DecisionSubstantially Equivalent, Oct 4, 2007
ReceivedSep 4, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K072465

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.