ClearanceBrief
510(k) K082801 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

PHANTOM PLUS CAGE SYSTEM

ApplicantUs Spine, Boca Raton FL, US
DecisionSubstantially Equivalent, Dec 22, 2008
ReceivedSep 24, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082801

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.