ClearanceBrief
510(k) K243461 ยท

Calibrate Interbody Systems

ApplicantAlphatec Spine, Inc., Carlsbad CA, US
DecisionSubstantially Equivalent, Mar 4, 2025
ReceivedNov 8, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K243461

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.