ClearanceBrief
510(k) K212489 ยท PML Bone Cement, Posterior Screw Augmentation

BonOs Inject Bone Cement; NEO Pedicle Screw System

ApplicantNeo Medical SA, Villette (Lavaux), CH
DecisionSubstantially Equivalent, Oct 28, 2021
ReceivedAug 9, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K212489

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.