ClearanceBrief
510(k) K153700 ยท OLO Orthopedic Stereotaxic Instrument

Aesculap(R) Implant Systems (AIS) S4 Navigation Instruments

ApplicantAesculap Implant Systems, LLC, Center Valley PA, US
DecisionSubstantially Equivalent, Jul 8, 2016
ReceivedDec 23, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K153700

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.