ClearanceBrief
510(k) K060249 ยท HWC Screw, Fixation, Bone

ULTRATINE FOREHEAD

ApplicantCoapt Systems, Inc., Palo Alto CA, US
DecisionSubstantially Equivalent, Jun 12, 2006
ReceivedJan 31, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060249

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.