ClearanceBrief
510(k) K231340 ยท NDN Cement, Bone, Vertebroplasty

Renova Spine Balloon Catheter

ApplicantBiopsybell S.R.L., Mirandola, IT
DecisionSubstantially Equivalent, Oct 30, 2023
ReceivedMay 9, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231340

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.