ClearanceBrief
510(k) K092825 ยท KWP Appliance, Fixation, Spinal Interlaminal

APEX SPINE SYSTEM 5.50 MM TITANIUM ROD & POLYAXIAL SCREW WASHER

ApplicantSpinecraft, Inc., Westchester IL, US
DecisionSubstantially Equivalent, Mar 16, 2010
ReceivedSep 11, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K092825

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.