ClearanceBrief
510(k) K031471 ยท KWP Appliance, Fixation, Spinal Interlaminal

ORIA SPINAL CLIP SYSTEM, LATERAL INTERMEDIATE CONNECTOR, MODEL AL01

ApplicantOrtho Tec, LLC, California CA, US
DecisionSubstantially Equivalent, Oct 10, 2003
ReceivedMay 9, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031471

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.