SoloPace Fusion Ground Pad

Basic Information

• Brand Name: SoloPace Fusion Ground Pad
• Primary DI: 00850056280006
• Version / Model: 705091001
• Company Name: SOLO PACE INC.
• Labeler DUNS: 138344845
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2026-02-05
• Public Version: 1
• Public Version Date: 2026-02-13
• Public Version Status: New
• Public Device Record Key: c6088e27-0d59-4802-9996-71477ec242bf

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: Yes
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
LDF	Electrode, Pacemaker, Temporary	Cardiovascular	870.3680	2

GMDN Terms

Code	Name	Definition	Implantable	Status
35224	External pacemaker, epicardial pacing	An external pulse generator (EPG) designed to generate periodic electrical cardiac pacing impulses and transmits them to the heart via invasive (percutaneous) leads to stimulate the heart when the sino-atrial (SA) node is not functioning properly or when the heart has a conductive disorder. It is commonly used: 1) in an emergency; 2) during surgery; or 3) following open-heart surgery until the heart recovers. It is not intended for defibrillation or cardioversion. The leads (not included) are inserted into the heart through a major vein (e.g., subclavian) or attached directly to the heart wall.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00850056280006	GS1

Premarket Submissions

Submission Number	Supplement Number
K252674	000