510(k) K212306

Device
Tapestry Biointegrative Implant
Applicant
Embody, Inc.
510(k) number
K212306
Product code
OWY
Decision
Substantially Equivalent (SESE)
Decision date
2021-11-02
Date received
2021-07-23
Regulation
878.3300
Classification name
Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Brianna Schehr
Address
4211 Monarch Way, Suite 500 Norfolk VA US 23508 23508

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code OWY

510(k)DeviceApplicantDecision date
K251690Arthrex SpeedFLEX™ ImplantArthrex, Inc.2025-09-30
K252647Tapestry Biointegrative ImplantEmbody, Inc.2025-09-19
K250109TYBR Collagen GelTybr Health2025-06-06
K243843Tendon Protect (50242)Kerecis Limited2025-06-04
K242631REGENETEN™ Bioinductive ImplantSmith & Nephew Inc., Endoscopy Div.2024-11-26
K222501Regeneten Bioinductive ImplantSmith and Nephew, Inc.2023-05-11
K220867Tapestry Biointegrative ImplantEmbody, Inc.2022-05-23
K201572TAPESTRY Biointegrative ImplantEmbody, Inc.2020-10-19
K151083BioBridge Collagen MatrixFibralign Corporation2016-01-08
K140300COLLAGEN TENDON SHEET-DDI (CTS-DDI)Rotation Medical, Inc.2014-03-26
K133169MESO TENDON MATRIXKensey Nash Corporation Dba Dsm Biomedical2013-12-20
K131143TRELLIS COLLAGEN RIBBONWrightmedicaltechnologyinc2013-10-07
K120479MTF FASCIAMusculoskeletal Transplant Foundation2012-11-08