FRS™CANNULATED SCREW 852025014

GUDID 00887868057557

Biomet Orthopedics, LLC

Orthopaedic bone screw, non-bioabsorbable, sterile
Primary Device ID00887868057557
NIH Device Record Key105f2c93-b017-4d23-8fa9-5b4554418e3e
Commercial Distribution StatusIn Commercial Distribution
Brand NameFRS™CANNULATED SCREW
Version Model Number8520-25-014
Catalog Number852025014
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 Datetrue
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

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868057557 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-24

On-Brand Devices [FRS™CANNULATED SCREW]

008878680577248520-30-034
008878680577178520-30-032
008878680577008520-30-030
008878680576948520-30-028
008878680576878520-30-026
008878680576708520-30-024
008878680576638520-30-022
008878680576568520-30-020
008878680576498520-30-018
008878680576328520-30-016
008878680576258520-30-014
008878680576188520-25-026
008878680576018520-25-024
008878680575958520-25-022
008878680575888520-25-020
008878680575718520-25-018
008878680575648520-25-016
008878680575578520-25-014
008878680575408520-25-012
008878680575338520-25-010

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