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Acera Surgical, Inc.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7
Categories3
Latest FDA decision2025-06-20
TypeNumberDevice NameCodeDateActions
510(k) K251224 Restrata Soft Tissue Reinforcement (STR)OXF2025-06-20 View
510(k) K223725 Restrata® MiniMatrixQSZ2023-05-18 View
510(k) K193583 Restrata®QSZ2020-09-25 View
510(k) K172603 Cerafix Dura SubstituteGXQ2017-11-27 View
510(k) K170300 Restrata Wound MatrixQSZ2017-04-26 View
510(k) K161278 Cerafix Dura SubstituteGXQ2016-08-08 View
510(k) K153613 Cerafix Dura SubstituteGXQ2016-03-16 View

Related Clinical Trials

NCT06578650A Prospective, Single-arm, Clinical Trial of Electrospun Fiber Matrix (Restrata) in the Treatment of Surgical Defects Secondary to Resection of Malignant Cutaneous NeoplasmsRECRUITING
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