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

ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

K Number: K993855 · Decision Dec 15, 1999
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
655
Applicant Total
56
Review Days
30

Basic Information

Device Name
ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM
K Number
K993855
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DANEK MEDICAL, INC.
Date Received
November 15, 1999
Decision Date
December 15, 1999
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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