ClearanceBrief
510(k) K073151 ยท NKB Thoracolumbosacral Pedicle Screw System

MANTIS SPINAL SYSTEM

ApplicantStryker Corp., Allendale NJ, US
DecisionSubstantially Equivalent, Dec 6, 2007
ReceivedNov 8, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K073151

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.