LOCON

GUDID 00840420132987

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile

Primary Device ID	00840420132987
NIH Device Record Key	7d0b7498-5e51-4461-8f1a-32607ceef977
Commercial Distribution Status	In Commercial Distribution
Brand Name	LOCON
Version Model Number	49000MDR
Company DUNS	807201207
Company Name	WRIGHT MEDICAL TECHNOLOGY, INC.
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	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	+1(800)238-7117
Email	customerservice@wmt.com
Phone	+1(800)238-7117
Email	customerservice@wmt.com
Phone	+1(800)238-7117
Email	customerservice@wmt.com
Phone	+1(800)238-7117
Email	customerservice@wmt.com
Phone	+1(800)238-7117
Email	customerservice@wmt.com
Phone	+1(800)238-7117
Email	customerservice@wmt.com
Phone	+1(800)238-7117
Email	customerservice@wmt.com
Phone	+1(800)238-7117
Email	customerservice@wmt.com
Phone	+1(800)238-7117
Email	customerservice@wmt.com

Device Dimensions

Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840420132987 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K994061

FDA Product Code

HRS	PLATE, FIXATION, BONE