FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

IOS EXTERNAL FIXATOR, MODEL 2-0-0

K Number: K070724 · Decision May 16, 2007
Classifications
1
FEI Numbers
247
Registration Numbers
247
Same Product Code
392
Applicant Total
3
Review Days
62

Basic Information

Device Name
IOS EXTERNAL FIXATOR, MODEL 2-0-0
K Number
K070724
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
INTELLIGENT ORTHOPAEDICS LTD
Date Received
March 15, 2007
Decision Date
May 16, 2007
Product Code
KTT
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
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

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