ClearanceBrief
510(k) K232023 ยท LDK Device, Sensing, Optical Contour

Momentum Spine

ApplicantMomentum Health, Inc., Montreal, CA
DecisionSubstantially Equivalent, Oct 4, 2023
ReceivedJul 7, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232023

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.