ClearanceBrief
510(k) K121671 ยท NKB Thoracolumbosacral Pedicle Screw System

PATHFINDER NXT MINIMALLY INVASIVE PEDICLE SCREW SYSTEM

ApplicantZimmer Spine, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Jul 18, 2012
ReceivedJun 6, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121671

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.