ClearanceBrief
510(k) K982908 ยท KWP Appliance, Fixation, Spinal Interlaminal

MODIFICATION TO EBI SPINELINK SYSTEM

ApplicantElectro-Biology, Inc., Parsippany NJ, US
DecisionSubstantially Equivalent, Aug 28, 1998
ReceivedAug 18, 1998
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K982908

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.