ClearanceBrief
510(k) K080504 ยท NKB Thoracolumbosacral Pedicle Screw System

PIONEER LOWTOP SPINAL ROD SYSTEM

ApplicantPioneer Surgical Technology, Marquette MI, US
DecisionSubstantially Equivalent, Mar 20, 2008
ReceivedFeb 25, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K080504

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.