ClearanceBrief
510(k) K071860 ยท NKB Thoracolumbosacral Pedicle Screw System

MODIFICATION TO: VIPER SPINE SYSTEM

ApplicantDepuy Spine, Inc., Raynham MA, US
DecisionSubstantially Equivalent, Aug 1, 2007
ReceivedJul 5, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K071860

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.