ClearanceBrief
510(k) K072729 ยท KWP Appliance, Fixation, Spinal Interlaminal

SIERRA

ApplicantSeaspine, Inc., Vista CA, US
DecisionSubstantially Equivalent, Apr 17, 2008
ReceivedSep 26, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K072729

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.