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

AVAflex Vertebral Balloon System

K Number: K151125 · Decision Nov 24, 2015
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
34
Review Days
210

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Basic Information

Device Name
AVAflex Vertebral Balloon System
K Number
K151125
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Care Fusion
Date Received
April 28, 2015
Decision Date
November 24, 2015
Product Code
HRX
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
HRX Arthroscope

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