ClearanceBrief
510(k) K062181 ยท KWP Appliance, Fixation, Spinal Interlaminal

C-JAWS CERVICAL COMPRESSIVE MINI FRAME

ApplicantMedicrea Technologies, Round Rock TX, US
DecisionSubstantially Equivalent, Jan 16, 2007
ReceivedJul 31, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062181

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.