ClearanceBrief
510(k) K990986 ยท KWP Appliance, Fixation, Spinal Interlaminal

CONTOUR SPINAL SYSTEM

ApplicantOrtho Development Corp., Draper UT, US
DecisionSubstantially Equivalent, Oct 14, 1999
ReceivedMar 24, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990986

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.