7 Hole VL Gridlock Fibula Plate

GUDID 00812926025438

TRILLIANT SURGICAL, LTD.

Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable, non-sterile
Primary Device ID00812926025438
NIH Device Record Key9e8d7d88-07cf-47b2-9a9b-6bea69a4f294
Commercial Distribution StatusIn Commercial Distribution
Brand Name7 Hole VL Gridlock Fibula Plate
Version Model Number300-60-001
Company DUNS828829072
Company NameTRILLIANT SURGICAL, 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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

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Device Identifiers

Device Issuing AgencyDevice ID
GS100812926025438 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRSPlate, Fixation, Bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


[00812926025438]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2017-03-13

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