ClearanceBrief
510(k) K071376 ยท NKB Thoracolumbosacral Pedicle Screw System

MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM

ApplicantVertebron, Inc., Stratford CT, US
DecisionSubstantially Equivalent, Jun 13, 2007
ReceivedMay 17, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K071376

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.