TAPERLOC COMPLETE 51-201040

GUDID 00880304506787

Biomet Orthopedics, LLC

Bone file/rasp, manual Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable

Primary Device ID	00880304506787
NIH Device Record Key	3cd9510d-41c0-47dc-98a4-61a027aa2514
Commercial Distribution Status	In Commercial Distribution
Brand Name	TAPERLOC COMPLETE
Version Model Number	51-201040
Catalog Number	51-201040
Company DUNS	129278169
Company Name	Biomet Orthopedics, LLC
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	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
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)348-9500
Email	customerservice@zimmerbiomet.com
Phone	+1(800)348-9500
Email	customerservice@zimmerbiomet.com
Phone	+1(800)348-9500
Email	customerservice@zimmerbiomet.com
Phone	+1(800)348-9500
Email	customerservice@zimmerbiomet.com
Phone	+1(800)348-9500
Email	customerservice@zimmerbiomet.com
Phone	+1(800)348-9500
Email	customerservice@zimmerbiomet.com
Phone	+1(800)348-9500
Email	customerservice@zimmerbiomet.com
Phone	+1(800)348-9500
Email	customerservice@zimmerbiomet.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 Identifiers

Device Issuing Agency	Device ID
GS1	00880304506787 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K120030

FDA Product Code

KWL	Prosthesis, hip, hemi-, femoral, metal