ClearanceBrief
510(k) K062785 ยท KWP Appliance, Fixation, Spinal Interlaminal

LTD POLYAXIAL FIXATION SYSTEM

ApplicantUs Spine, Apple Valley MN, US
DecisionSubstantially Equivalent, Dec 26, 2006
ReceivedSep 18, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K062785

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.