ClearanceBrief
510(k) K043473 ยท KWP Appliance, Fixation, Spinal Interlaminal

MODIFICATION TO XIA SPINAL SYSTEM

ApplicantStryker Spine, Allendale NJ, US
DecisionSubstantially Equivalent, Jan 12, 2005
ReceivedDec 16, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K043473

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.