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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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