ClearanceBrief
510(k) K142041 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

POROSTEON PHUSION METAL CERVICAL CAGE

ApplicantPorosteon, Inc., Notre-Dame-De-L'Lle-Perrot,Quebec, CA
DecisionSubstantially Equivalent, Dec 19, 2014
ReceivedJul 28, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142041

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.