ClearanceBrief
510(k) K861622 ยท IKK System, Isokinetic Testing And Evaluation

SAGITTAL & ROTARY ACT/PASS KNEE LIGAMENT TESTER

ApplicantOrthopedic Systems, Inc., Hayward CA, US
DecisionSubstantially Equivalent, May 27, 1986
ReceivedApr 29, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861622

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.