ClearanceBrief
510(k) K071945 ยท NKB Thoracolumbosacral Pedicle Screw System

S4 SPINAL SYSTEM

ApplicantAesculap Implant Systems, Center Valley PA, US
DecisionSubstantially Equivalent, Sep 20, 2007
ReceivedJul 13, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K071945

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.