ClearanceBrief
510(k) K991198 ยท KWP Appliance, Fixation, Spinal Interlaminal

DYNA-LOK PLUS SPINAL SYSTEM

ApplicantSofamor Danek USA,Inc., Memphis TN, US
DecisionSubstantially Equivalent, Aug 27, 1999
ReceivedApr 8, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K991198

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.