ClearanceBrief
510(k) K232345 ยท OLO Orthopedic Stereotaxic Instrument

ATEC Posterior Navigated Disc Prep Instruments

ApplicantAlphatec Spine, Inc., Carlsbad CA, US
DecisionSubstantially Equivalent, Nov 2, 2023
ReceivedAug 4, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232345

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.