ClearanceBrief
510(k) K931208 ยท KWP Appliance, Fixation, Spinal Interlaminal

LOW PROFILE SLEAVE NUT ASSEMBLY

ApplicantAdvanced Spine Fixation Systems, Inc., Cypress CA, US
DecisionSubstantially Equivalent for Some Indications, Mar 28, 1994
ReceivedMar 10, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K931208

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.