ClearanceBrief
510(k) K090657 ยท NKB Thoracolumbosacral Pedicle Screw System

MODIFICATION TO: S4 SPINAL SYSTEM

ApplicantAesculap Implant Systems, Center Valley PA, US
DecisionSubstantially Equivalent, Apr 20, 2009
ReceivedMar 12, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K090657

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.