Threshold V2 Pedicular Fixation System 570-8560

GUDID M7405708560

Reduction Screw, Uncoated

SPINEOLOGY INC.

Spinal bone screw, non-bioabsorbable
Primary Device IDM7405708560
NIH Device Record Keyaef0a257-2bbe-4ce1-9193-58c5df300c36
Commercial Distribution StatusIn Commercial Distribution
Brand NameThreshold V2 Pedicular Fixation System
Version Model Number10-10-84-10
Catalog Number570-8560
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)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com
Phone+1(651)259-8500
Emailinfo@spineology.com

Device Dimensions

Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0
Length60 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM7405708560 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MNIORTHOSIS, SPINAL PEDICLE FIXATION

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


[M7405708560]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2024-07-22
Device Publish Date2017-04-25

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M7405705540Reduction Screw, Uncoated
M7405705535Reduction Screw, Uncoated
M7405705530Reduction Screw, Uncoated
M7405705050Reduction Screw, Uncoated
M7405705045Reduction Screw, Uncoated
M7405705040Reduction Screw, Uncoated
M7405705035Reduction Screw, Uncoated
M7405705030Reduction Screw, Uncoated

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