ClearanceBrief
510(k) K122352 ยท NKB Thoracolumbosacral Pedicle Screw System

NUVASIVE PRECEPT SPINAL SYSTEM

ApplicantNuvasive, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Sep 11, 2012
ReceivedAug 3, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K122352

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.