ClearanceBrief
510(k) K133529 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

CAMBER SPINE COVERIS CERVICAL CAGE

ApplicantCamber Spine, Newtown Square PA, US
DecisionSubstantially Equivalent, Mar 20, 2014
ReceivedNov 15, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K133529

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.