ClearanceBrief
510(k) K955540 ยท LXM Manipulator, Plunger-Like Joint

HAND HELD ATLAS INSTRUMENT

ApplicantSpinalight, Inc., Woodstock GA, US
DecisionSubstantially Equivalent, Mar 4, 1996
ReceivedDec 5, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K955540

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.