510(k) K222501

Device
Regeneten Bioinductive Implant
Applicant
Smith and Nephew, Inc.
510(k) number
K222501
Product code
OWY
Decision
Substantially Equivalent (SESE)
Decision date
2023-05-11
Date received
2022-08-18
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
Jenna Horsley
Address
150 Minuteman Rd. Andover MA US 01810 01810

FDA Registration Numbers

Source Documents

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

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