Tower Screw Caddy Assembly

GUDID M739164017032

TowerLOX EXT Tower Screw Caddy Assembly

CAPTIVA SPINE, INC.

Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable
Primary Device IDM739164017032
NIH Device Record Key65cdb76a-8cdb-481c-a2b4-9b6340b95677
Commercial Distribution StatusIn Commercial Distribution
Brand NameTower Screw Caddy Assembly
Version Model Number16401-7032
Company DUNS836975784
Company NameCAPTIVA SPINE, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM739164017032 [Primary]

FDA Product Code

FSMTray, Surgical, Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


[M739164017032]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-09
Device Publish Date2023-09-29

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M73910110250 - TransFasten - LSF (Lateral Sacroiliac Fusion System)2024-03-11 Sacroiliac Immobilization Device - 9mm (D) x 25mm (L)
M73910110300 - TransFasten - LSF (Lateral Sacroiliac Fusion System)2024-03-11 Sacroiliac Immobilization Device - 9mm (D) x 30mm (L)
M73910110350 - TransFasten - LSF (Lateral Sacroiliac Fusion System)2024-03-11 Sacroiliac Immobilization Device - 9mm (D) x 35mm (L)
M73910110400 - TransFasten - LSF (Lateral Sacroiliac Fusion System)2024-03-11 Sacroiliac Immobilization Device - 9mm (D) x 40mm (L)

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