ClearanceBrief
510(k) K012516 ยท KWP Appliance, Fixation, Spinal Interlaminal

EBI SPINELINK - II SPINAL FIXATION SYSTEM

ApplicantEbi, L.P., Parsippany NJ, US
DecisionSubstantially Equivalent, Nov 27, 2001
ReceivedAug 6, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K012516

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.