TAPERLOC COMPLETE MICROPLASTY 51-208250

GUDID 00880304747784

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	00880304747784
NIH Device Record Key	17ccab13-29c6-4f6e-b632-dba10806d95f
Commercial Distribution Status	In Commercial Distribution
Brand Name	TAPERLOC COMPLETE MICROPLASTY
Version Model Number	51-208250
Catalog Number	51-208250
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	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)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 Identifiers

Device Issuing Agency	Device ID
GS1	00880304747784 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K110400

FDA Product Code

KWY	Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented