ClearanceBrief
510(k) K020155 ยท KWP Appliance, Fixation, Spinal Interlaminal

DYNA-LOK CLASSIC SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Feb 5, 2002
ReceivedJan 17, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K020155

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.