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

MODIFICATION TO REFLEX ANTERIOR CERVICAL PLATE SYSTEM

K Number: K020650 · Decision Mar 29, 2002
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
655
Applicant Total
208
Review Days
29

Basic Information

Device Name
MODIFICATION TO REFLEX ANTERIOR CERVICAL PLATE SYSTEM
K Number
K020650
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HOWMEDICA OSTEONICS CORP.
Date Received
February 28, 2002
Decision Date
March 29, 2002
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

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