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

SPINE SYSTEM EVOLUTION

K Number: K001080 · Decision Jun 29, 2000
Classifications
1
FEI Numbers
330
Registration Numbers
330
Same Product Code
429
Applicant Total
174
Review Days
86

Basic Information

Device Name
SPINE SYSTEM EVOLUTION
K Number
K001080
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AESCULAP, INC.
Date Received
April 4, 2000
Decision Date
June 29, 2000
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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