Fortress Rod 640-7035

GUDID M7406407035

Pedicle Screw

SPINEOLOGY INC.

Bone-screw internal spinal fixation system rod
Primary Device IDM7406407035
NIH Device Record Key2d9266f9-4369-4173-9d0b-1bcbb72d3504
Commercial Distribution StatusIn Commercial Distribution
Brand NameFortress Rod
Version Model Number10-10-48-44
Catalog Number640-7035
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

Device Dimensions

Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter
Device Size Text, specify0
Length35 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM7406407035 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NKBOrthosis, spinal pedicle fixation, for degenerative disc disease

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


[M7406407035]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2024-07-22
Device Publish Date2015-04-17

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