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

ARTHROCARE PERCD SPINEWAND

K Number: K030954 · Decision Apr 16, 2003
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
112
Review Days
20

Basic Information

Device Name
ARTHROCARE PERCD SPINEWAND
K Number
K030954
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ARTHROCARE CORP.
Date Received
March 27, 2003
Decision Date
April 16, 2003
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

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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