ClearanceBrief
510(k) K153396 ยท OLO Orthopedic Stereotaxic Instrument

Aesculap OrthoPilot Next Generation

ApplicantAesculap Implant Systems, LLC, Center Valley PA, US
DecisionSubstantially Equivalent, May 16, 2016
ReceivedNov 24, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K153396

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.