510(k) K223538

Integrity Implant by Anika Therapeutics, Inc. — Product Code OWX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 17, 2023
Date Received
November 23, 2022
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mesh, Surgical, Non-Absorbable, Orthopaedics, Reinforcement Of Tendon
Device Class
Class II
Regulation Number
878.3300
Review Panel
OR
Submission Type

For reinforcement of soft tissue where weakness exists in tendon repair.