Aurora Trial Plate 19

GUDID 09348215067106

SIGNATURE ORTHOPAEDICS PTY LTD

Surgical implant template, reusable
Primary Device ID09348215067106
NIH Device Record Key8be86f5f-e6c4-43b6-bd7e-c3429d070e8f
Commercial Distribution StatusIn Commercial Distribution
Brand NameAurora Trial Plate 19
Version Model Number132-16-0111
Company DUNS751993028
Company NameSIGNATURE ORTHOPAEDICS PTY LTD
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 Usefalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS109348215067106 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWQAppliance, Fixation, Spinal Intervertebral Body

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[09348215067106]

Moist Heat or Steam Sterilization


[09348215067106]

Moist Heat or Steam Sterilization


[09348215067106]

Moist Heat or Steam Sterilization


[09348215067106]

Moist Heat or Steam Sterilization


[09348215067106]

Moist Heat or Steam Sterilization


[09348215067106]

Moist Heat or Steam Sterilization


[09348215067106]

Moist Heat or Steam Sterilization


[09348215067106]

Moist Heat or Steam Sterilization


[09348215067106]

Moist Heat or Steam Sterilization


[09348215067106]

Moist Heat or Steam Sterilization


[09348215067106]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-08
Device Publish Date2020-06-30

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