ClearanceBrief
510(k) K210275 ยท NKB Thoracolumbosacral Pedicle Screw System

Polaris Spinal System

ApplicantZimmer Biomet Spine, Inc., Westminister CO, US
DecisionSubstantially Equivalent, Apr 2, 2021
ReceivedFeb 1, 2021
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K210275

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.