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18 : 275278 Curti D, Dagani F, Galmozzi MR, Marzatico F

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Subject to the applicant adequately addressing this concern, we would agree with the applicant that the technology meets the cost criterion and are therefore proposing to approve the Aveir TM Dual-Chamber Leadless Pacemaker for new technology add-on payments for FY 2024, subject to the technology receiving FDA marketing authorization as a Breakthrough Device for the indication corresponding to the Breakthrough Device designation by July 1, 2023

83 Zhongs team isolated and cultured human ectopic endometrial stromal cells (HEcESCs) from fresh ectopic endometrial tissue (ovarian endometrial tumor wall) of patients diagnosed with ovarian endometriosis