KangLi Locking Plates System T4071010

GUDID 06937762166511

Tibial Locking Plates 10 holes

Suzhou Kangli Orthopaedics Instrument Co.,Ltd.

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Primary Device ID	06937762166511
NIH Device Record Key	86e20cb6-e228-4b27-80b1-8c142887fc47
Commercial Distribution Status	In Commercial Distribution
Brand Name	KangLi Locking Plates System
Version Model Number	T4071010
Catalog Number	T4071010
Company DUNS	527054774
Company Name	Suzhou Kangli Orthopaedics Instrument Co.,Ltd.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Dimensions

Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
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Length	191 Millimeter
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Length	191 Millimeter
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Length	191 Millimeter
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Length	191 Millimeter
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Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0
Length	191 Millimeter
Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	06937762166511 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K133840

FDA Product Code

HWC	Screw, Fixation, Bone