ClearanceBrief
510(k) K031452 ยท KWP Appliance, Fixation, Spinal Interlaminal

ORIA SPINAL CLIP SYSTEM, SACRAL CONNECTOR, MODELS CA03 AND AO03

ApplicantOrtho Tec, LLC, California CA, US
DecisionSubstantially Equivalent, Jun 18, 2003
ReceivedMay 7, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K031452

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.