ClearanceBrief
510(k) K072415 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

STALIF (TM) C

ApplicantSurgicraft , Ltd., Douglassville PA, US
DecisionSubstantially Equivalent, Jan 25, 2008
ReceivedAug 28, 2007
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K072415

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.