Threshold Curved Rod 530-2090

GUDID M7405302090

Curved Rod

SPINEOLOGY INC.

Bone-screw internal spinal fixation system rod
Primary Device IDM7405302090
NIH Device Record Keyc9d03888-94bb-47df-aec1-664d79ed7dd5
Commercial Distribution StatusIn Commercial Distribution
Brand NameThreshold Curved Rod
Version Model Number10-10-08-13
Catalog Number530-2090
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

Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0
Length90 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM7405302090 [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

[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


[M7405302090]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2024-07-23
Device Publish Date2015-01-09

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