ClearanceBrief
510(k) K014296 ยท KWP Appliance, Fixation, Spinal Interlaminal

CD HORIZON SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Dec 10, 2002
ReceivedDec 31, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K014296

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.