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

ARCUATE VERTEBRAL AUGMENTATION SYSTEM

K Number: K070527 · Decision May 4, 2007
Classifications
1
FEI Numbers
112
Registration Numbers
112
Same Product Code
106
Applicant Total
145
Review Days
70

Basic Information

Device Name
ARCUATE VERTEBRAL AUGMENTATION SYSTEM
K Number
K070527
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDTRONIC SOFAMOR DANEK
Date Received
February 23, 2007
Decision Date
May 4, 2007
Product Code
NDN
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
NDN Cement, Bone, Vertebroplasty

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