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

MODIFICATION TO MACS MODULAR ANTERIOR CONSTRUCT SYSTEM

K Number: K032059 · Decision Jul 25, 2003
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
655
Applicant Total
174
Review Days
23

Basic Information

Device Name
MODIFICATION TO MACS MODULAR ANTERIOR CONSTRUCT SYSTEM
K Number
K032059
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AESCULAP, INC.
Date Received
July 2, 2003
Decision Date
July 25, 2003
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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