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

MSD WIRE SYSTEM

K Number: K020426 · Decision Feb 26, 2002
Classifications
1
FEI Numbers
330
Registration Numbers
330
Same Product Code
429
Applicant Total
96
Review Days
18

Basic Information

Device Name
MSD WIRE SYSTEM
K Number
K020426
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDTRONIC SOFAMOR DANEK, INC.
Date Received
February 8, 2002
Decision Date
February 26, 2002
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

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