ClearanceBrief
510(k) K895978 ยท KWP Appliance, Fixation, Spinal Interlaminal

CHIBA SPINAL SYSTEM

ApplicantDanek Medical, Inc., Memphis TN, US
DecisionSubstantially Equivalent, Aug 9, 1990
ReceivedOct 12, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895978

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.