ClearanceBrief
510(k) K102313 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

PATRIOT TRANSCONTINENTAL M SPACERS

ApplicantGlobus Medical, Inc., Audubon PA, US
DecisionSubstantially Equivalent, Dec 3, 2010
ReceivedAug 16, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K102313

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.