ClearanceBrief
510(k) K964517 ยท IYE Accelerator, Linear, Medical

LINAC SCALPEL FLOORSTAND

ApplicantSurgical Navigation Technologies, Inc., Broomfield CO, US
DecisionSubstantially Equivalent, Apr 1, 1997
ReceivedNov 12, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K964517

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.