Class Class U

Restrata® MiniMatrix (K223725)

K223725 2023-05-18 Traditional
Home/ Devices/ Restrata® MiniMatrix (K223725)

Description

Restrata® MiniMatrix by Acera Surgical, Inc. — FDA 510(k) cleared unknown device.

Regulatory Information

Device ClassClass Class U
510(k) NumberK223725
Clearance Date2023-05-18
Clearance TypeTraditional
Product CodeQSZ

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