ClearanceBrief
510(k) K122444 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

CERVICAL CAGE

ApplicantEisertech, LLC, San Diego CA, US
DecisionSubstantially Equivalent, Aug 30, 2012
ReceivedAug 10, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K122444

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.