DARCO

GUDID 00840420136732

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile

Primary Device ID	00840420136732
NIH Device Record Key	f36ce5b4-c9ca-4184-8d72-5ba7c58d3efb
Commercial Distribution Discontinuation	2016-03-07
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	DARCO
Version Model Number	NO2825030
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
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 Identifiers

Device Issuing Agency	Device ID
GS1	00840420136732 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K022325

FDA Product Code

HRS	PLATE, FIXATION, BONE