ClearanceBrief
510(k) K233899 · SBF Orthopedic Augmented Reality

Knee+

ApplicantPixee Medical, Besançon, FR
DecisionSubstantially Equivalent, Mar 8, 2024
ReceivedDec 11, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233899

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.