ClearanceBrief
510(k) K870830 ยท KWP Appliance, Fixation, Spinal Interlaminal

WARSAW ORTHOPEDIC TSR CROSS LINK SYSTEM

ApplicantWarsaw Orthopedic, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, May 4, 1987
ReceivedMar 3, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K870830

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.