ClearanceBrief
510(k) K092631 ยท NKB Thoracolumbosacral Pedicle Screw System

MANTIS REDUX SPINAL SYSTEM

ApplicantStryker Spine, Allendale NJ, US
DecisionSubstantially Equivalent, Sep 25, 2009
ReceivedAug 26, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K092631

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.