ClearanceBrief
510(k) K990959 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM

ApplicantSpineology, Inc., Stillwater MN, US
DecisionSubstantially Equivalent, Dec 27, 1999
ReceivedMar 22, 1999
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K990959

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.