F³ FRAGMENT PLATING SYSTEMSMALL FRAG LOCKING PLATE, HIGH STRENGTH STRAIGHT 131217002

GUDID 00887868012495

Biomet Orthopedics, LLC

Orthopaedic fixation plate, non-bioabsorbable, non-sterile
Primary Device ID00887868012495
NIH Device Record Key8f2b6fb4-3d6f-49f5-808f-392a890eddb1
Commercial Distribution StatusIn Commercial Distribution
Brand NameF³ FRAGMENT PLATING SYSTEMSMALL FRAG LOCKING PLATE, HIGH STRENGTH STRAIGHT
Version Model Number1312-17-002
Catalog Number131217002
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868012495 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LXTAPPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


[00887868012495]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-01-14
Device Publish Date2015-10-24

Devices Manufactured by Biomet Orthopedics, LLC

00887868254451 - Comprehensive® Reverse Shoulder2024-11-21
00887868578250 - Comprehensive®2024-11-13
08428898885684 - BIPASS DISPOSABLE PUSHER2024-09-11
08428898885691 - BIPASS DISPOSABLE PUSHER2024-09-11
00880304338548 - AGC ANTERIOR FILE2024-09-11
00880304339224 - PARALLEL PULLER2024-09-11
00880304342187 - AGC MODULAR TIBIAL II2024-09-11
00880304365247 - BIO-MODULAR2024-09-11

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.