THINFLAP SYSTEM 5/PK 91-6604-5PK

GUDID 00841036138233

BIOMET MICROFIXATION, 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
Primary Device ID00841036138233
NIH Device Record Keyedaf2578-9857-46cf-aac5-5b4ad1bc9552
Commercial Distribution StatusIn Commercial Distribution
Brand NameTHINFLAP SYSTEM 5/PK
Version Model Number91-6604-5PK
Catalog Number91-6604-5PK
Company DUNS046189866
Company NameBIOMET MICROFIXATION, INC
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(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100841036138233 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GXRCOVER, BURR HOLE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


[00841036138233]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-11

On-Brand Devices [THINFLAP SYSTEM 5/PK]

0084103619040891-6804-5PK
0084103613823391-6604-5PK
0088823302531791-6804-5PK
0088823301226391-6604-5PK

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