ClearanceBrief
510(k) K023415 ยท KWP Appliance, Fixation, Spinal Interlaminal

MODIFICATION TO DYNALOK CLASSIC SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Dec 13, 2002
ReceivedOct 11, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K023415

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.