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

ARTHREX OPES ELECTRODES AND ACCESSORIES

K Number: K023986 · Decision Dec 17, 2002
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
348
Review Days
15

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Basic Information

Device Name
ARTHREX OPES ELECTRODES AND ACCESSORIES
K Number
K023986
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrex, Inc.
Date Received
December 2, 2002
Decision Date
December 17, 2002
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
Y

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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Other Clearances by Arthrex, Inc.

K Number Device Name
K253931 Arthrex Bioabsorbable PushLock Suture Anchors
K254215 Arthrex Beaming System
K252016 Arthrex Humeral Nails
K260561 Arthrex FiberTak Suture Anchor
K260405 FiberTape Button
K252196 Arthrex FibuLock Nail System
K260353 Arthrex Humeral Plating System (Anatomic Humeral Plate) and Cerclage Button
K254229 Arthrex Nano FiberTak Suture Anchor
K253713 Arthrex Variable Angle (VA) Proximal Tibia Plating System
K252807 Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates
Search all 348 clearances from Arthrex, Inc. →