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

SMITH + NEPHEW RF ARTHROSCOPIC WAND SYSTEM

K Number: K001226 · Decision Jun 26, 2000
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
669
Applicant Total
423
Review Days
70

Basic Information

Device Name
SMITH + NEPHEW RF ARTHROSCOPIC WAND SYSTEM
K Number
K001226
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SMITH & NEPHEW, INC.
Date Received
April 17, 2000
Decision Date
June 26, 2000
Product Code
HRX
Advisory Committee
Orthopedic
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
HRX Arthroscope

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