ClearanceBrief
510(k) K083637 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

CALIX SPINAL IMPLANT SYSTEM

ApplicantX-Spine Systems, Inc., Miamisburg OH, US
DecisionSubstantially Equivalent, Apr 20, 2009
ReceivedDec 9, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K083637

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.