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
249
Registration Numbers
249
Same Product Code
403
Applicant Total
3
Review Days
62

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KTT), ordered by most recent decision date.

View all

Other Clearances by Intelligent Orthopaedics, Ltd.

K Number Device Name
K111001 STERILE STORM (R) OPERATING KIT
K061607 STORM OPERATING KIT, MODEL 1-10-0