ClearanceBrief
510(k) K934007 ยท KWP Appliance, Fixation, Spinal Interlaminal

SOFAMOR ORFIL SPINE FIXATION SYSTEM

ApplicantSofamor Co., France, FR
DecisionSubstantially Equivalent, Jun 2, 1994
ReceivedAug 18, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934007

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.