FDA 510(k) Applications Submitted by ACERA SURGICAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K193583 12/23/2019 Restrata« Acera Surgical, Inc.
K161278 05/06/2016 Cerafix Dura Substitute ACERA SURGICAL, INC.
K172603 08/30/2017 Cerafix Dura Substitute Acera Surgical, Inc.
K153613 12/17/2015 Cerafix Dura Substitute ACERA SURGICAL, INC.
K170300 01/31/2017 Restrata Wound Matrix Acera Surgical, Inc.
K223725 12/13/2022 Restrata« MiniMatrix Acera Surgical, Inc.


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