7mm Twist Subtalar Implant

GUDID 00812926020235

TRILLIANT SURGICAL, LTD.

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Primary Device ID	00812926020235
NIH Device Record Key	0f718330-5b01-4ec0-846a-992917fd1923
Commercial Distribution Status	In Commercial Distribution
Brand Name	7mm Twist Subtalar Implant
Version Model Number	102-10-007
Company DUNS	828829072
Company Name	TRILLIANT SURGICAL, LTD.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Dimensions

Width	7 Millimeter
Width	7 Millimeter
Width	7 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter
Height	12.75 Millimeter
Width	7 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812926020235 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K103183

FDA Product Code

HWC	Screw, Fixation, Bone