ClearanceBrief
510(k) K093206 ยท OLO Orthopedic Stereotaxic Instrument

ORTHOMAP 3D 1.1 MODULE

ApplicantStryker Corp., Freiburg, DE
DecisionSubstantially Equivalent, Aug 4, 2010
ReceivedOct 13, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K093206

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.