Fortress Set Screw 640-5000

GUDID M7406405000

Set Screw

SPINEOLOGY INC.

Spinal bone set screw
Primary Device IDM7406405000
NIH Device Record Key2b5022dd-e757-479d-8a37-66cb8ca3ad17
Commercial Distribution StatusIn Commercial Distribution
Brand NameFortress Set Screw
Version Model Number10-10-53-1
Catalog Number640-5000
Company DUNS033014361
Company NameSPINEOLOGY INC.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com
Phone+1(651)256-8500
Emailinfo@spineology.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM7406405000 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MNIORTHOSIS, SPINAL PEDICLE FIXATION

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


[M7406405000]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2024-07-22
Device Publish Date2014-12-05

On-Brand Devices [Fortress Set Screw]

M7406406000Set Screw
M7406405000Set Screw

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