Contact PEEK IBF System 34-TRL36-10-4

GUDID 00846468036980

TRIAL SPACER

Pioneer Surgical Technology, Inc.

Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable

• Primary Device ID: 00846468036980
• NIH Device Record Key: abf5681e-7639-4d13-98b4-f35bfa255a53
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Contact PEEK IBF System
• Version Model Number: 34-TRL36-10-4
• Catalog Number: 34-TRL36-10-4
• Company DUNS: 793384496
• Company Name: Pioneer Surgical Technology, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com
• Phone: +1(386)418-8888
• Email: labeling@rtix.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00846468031213 [Primary]
GS1	00846468036980 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

[00846468036980]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-12-30
• Device Publish Date: 2019-12-21

On-Brand Devices [Contact PEEK IBF System]

• 00846468037482: WINDOW INSERTER
• 00846468037475: WINDOW INSERTER
• 00846468037468: WINDOW INSERTER
• 00846468037451: DISTRACTION WINDOW
• 00846468037444: DISTRACTION WINDOW
• 00846468037437: DISTRACTION WINDOW
• 00846468037420: DISTRACTION WINDOW
• 00846468037413: DISTRACTION WINDOW
• 00846468037406: DISTRACTION WINDOW
• 00846468037390: DISTRACTION WINDOW
• 00846468037383: DISTRACTION WINDOW
• 00846468037376: DISTRACTION WINDOW
• 00846468037369: DISTRACTION WINDOW
• 00846468037352: DISTRACTION WINDOW
• 00846468037345: DISTRACTION WINDOW
• 00846468037338: DISTRACTION WINDOW
• 00846468037321: DISTRACTION WINDOW
• 00846468037314: DISTRACTION WINDOW
• 00846468037291: TRIAL SPACER
• 00846468037284: TRIAL SPACER
• 00846468037277: TRIAL SPACER
• 00846468037260: TRIAL SPACER
• 00846468037253: TRIAL SPACER
• 00846468037246: TRIAL SPACER
• 00846468037239: TRIAL SPACER
• 00846468037222: TRIAL SPACER
• 00846468037215: TRIAL SPACER
• 00846468037208: TRIAL SPACER
• 00846468037192: TRIAL SPACER
• 00846468037185: TRIAL SPACER
• 00846468037178: TRIAL SPACER
• 00846468037161: TRIAL SPACER
• 00846468037154: TRIAL SPACER
• 00846468037147: TRIAL SPACER
• 00846468037130: TRIAL SPACER
• 00846468037123: TRIAL SPACER
• 00846468037116: TRIAL SPACER
• 00846468037109: TRIAL SPACER
• 00846468037093: TRIAL SPACER
• 00846468037086: TRIAL SPACER
• 00846468037079: TRIAL SPACER
• 00846468037062: TRIAL SPACER
• 00846468037055: TRIAL SPACER
• 00846468037048: TRIAL SPACER
• 00846468037031: TRIAL SPACER
• 00846468037024: TRIAL SPACER
• 00846468037017: TRIAL SPACER
• 00846468037000: TRIAL SPACER
• 00846468036997: TRIAL SPACER
• 00846468036980: TRIAL SPACER