ClearanceBrief
510(k) K120327 ยท OTO Mesh, Surgical, Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed

VERTESSA

ApplicantCaldera Medical, Inc., Agoura Hills CA, US
DecisionSubstantially Equivalent, May 10, 2012
ReceivedFeb 2, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120327

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.