FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Arthrex SpeedFLEX™ Implant

K Number: K251690 · Decision Sep 30, 2025
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
13
Applicant Total
348
Review Days
120

Basic Information

Device Name
Arthrex SpeedFLEX™ Implant
K Number
K251690
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrex, Inc.
Date Received
June 2, 2025
Decision Date
September 30, 2025
Product Code
OWY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OWY Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon

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