FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ARTHREX AR-8200 SHAVER SYSTEM

K Number: K932699 · Decision Jan 25, 1994
Classifications
1
FEI Numbers
387
Registration Numbers
387
Same Product Code
75
Applicant Total
348
Review Days
236

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Basic Information

Device Name
ARTHREX AR-8200 SHAVER SYSTEM
K Number
K932699
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Arthrex, Inc.
Date Received
June 3, 1993
Decision Date
January 25, 1994
Product Code
HWE
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
HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment

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K Number Device Name
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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
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