ClearanceBrief
510(k) K132991 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

C-BOX PEEK CERVICAL IBF

ApplicantInnovasis, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Feb 12, 2014
ReceivedSep 24, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K132991

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.