ClearanceBrief
510(k) K091234 ยท NDN Cement, Bone, Vertebroplasty

SKELTEX ISV

ApplicantSkeltex Technologies, Inc., Boucherville, Quebec, CA
DecisionSubstantially Equivalent, Feb 16, 2010
ReceivedApr 27, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K091234

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.