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FDA 510(k), K220867, Tapestry Biointegrative Implant
FDA 510(k), K220867, Tapestry Biointegrative Implant
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510(K) Number: K220867
Device Name: Tapestry Biointegrative Implant
Manufacturer: Embody, Inc.
Device Classification Name: Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon
Regulation Number: 878.3300
Classification Product Code: OWY
Date Received: 03/25/2022
Decision Date: 05/23/2022
Regulation Medical Specialty: General & Plastic Surgery
Device Name: Tapestry Biointegrative Implant
Manufacturer: Embody, Inc.
Device Classification Name: Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon
Regulation Number: 878.3300
Classification Product Code: OWY
Date Received: 03/25/2022
Decision Date: 05/23/2022
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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