ClearanceBrief
510(k) K113654 ยท KWP Appliance, Fixation, Spinal Interlaminal

CASPIAN

ApplicantK2m, Inc., Leesburg VA, US
DecisionSubstantially Equivalent, Jan 12, 2012
ReceivedDec 12, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K113654

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.