Rampart-O 270-0014

GUDID M7402700014

Distractor Paddle, 14 mm

SPINEOLOGY INC.

Surgical implant template, reusable
Primary Device IDM7402700014
NIH Device Record Key8c582c2e-864e-4f33-8024-572f7ef7ad6f
Commercial Distribution StatusIn Commercial Distribution
Brand NameRampart-O
Version Model Number83-05-01-14
Catalog Number270-0014
Company DUNS033014361
Company NameSPINEOLOGY INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com

Device Dimensions

Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter
Height14 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM7402700014 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


[M7402700014]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-06-11
Device Publish Date2024-06-03

On-Brand Devices [Rampart-O]

M7402700013Distractor Paddle, 13 mm
M7402700012Distractor Paddle, 12 mm
M7402700011Distractor Paddle, 11 mm
M7402700010Distractor Paddle, 10 mm
M7402700009Distractor Paddle, 9 mm
M7402700008Distractor Paddle, 8 mm
M7402700007Distractor Paddle, 7 mm
M7402700016Distractor Paddle, 16 mm
M7402700015Distractor Paddle, 15 mm
M7402700014Distractor Paddle, 14 mm
M7402500041Rampart Remover
M7402700021Slap Mallet Extension

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