Nevro ACCK7200

GUDID 00813426020503

IPG2000 Template Kit

NEVRO CORP.

Surgical implant template, single-use Surgical implant template, single-use Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable Medical ruler, reusable

• Primary Device ID: 00813426020503
• NIH Device Record Key: fac4f807-3375-446f-bbee-786a88ac6cd5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nevro
• Version Model Number: ACCK7200
• Catalog Number: ACCK7200
• Company DUNS: 926599155
• Company Name: NEVRO CORP.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com
• Phone: 9502510005
• Email: info@nevro.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813426020503 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P130022

FDA Product Code

• LGW: Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-01-22
• Device Publish Date: 2018-01-08

On-Brand Devices [Nevro]

• 00813426020510: Senza II
• 00813426020503: IPG2000 Template Kit
• 00813426020411: Passing Elevator Accessory Tool