FDA 510(k), K212306, Tapestry Biointegrative Implant

FDA 510(k), K212306, Tapestry Biointegrative Implant

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510(K) Number: K212306
Device Name: Tapestry Biointegrative Implant
Manufacturer: Brianna Schehr
Device Classification Name: Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon
Regulation Number: OWY
Classification Product Code: 07/23/2021
Date Received: 11/02/2021
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic

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