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

DIAMOND ANTERIOR CERVICAL PLATE SYSTEM

K Number: K100265 · Decision May 13, 2010
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
655
Applicant Total
11
Review Days
104

Basic Information

Device Name
DIAMOND ANTERIOR CERVICAL PLATE SYSTEM
K Number
K100265
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AMENDIA, INC.
Date Received
January 29, 2010
Decision Date
May 13, 2010
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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