ClearanceBrief
510(k) K093998 ยท OLO Orthopedic Stereotaxic Instrument

KNEEALIGN SYSTEM WITH REFERENCE SENSOR

ApplicantOrthalign, Inc., Newport Beach CA, US
DecisionSubstantially Equivalent, Mar 22, 2010
ReceivedDec 28, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K093998

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.