ClearanceBrief
510(k) K233332 · NKG Posterior Cervical Screw System

Statera-C™ Spinal System

ApplicantK&J Consulting Corp., Lansdale PA, US
DecisionSubstantially Equivalent, Nov 27, 2023
ReceivedSep 29, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233332

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.