ClearanceBrief
510(k) K945022 ยท KWP Appliance, Fixation, Spinal Interlaminal

APOFIX CERVICAL SPINE FIXATION

ApplicantSofamor Co., Berck/Mer, FR
DecisionSubstantially Equivalent for Some Indications, May 15, 1995
ReceivedOct 13, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K945022

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.