KneeKG system

Basic Information

• Brand Name: KneeKG system
• Primary DI: 00627843933236
• Version / Model: 0
• Catalog Number: P-142
• Company Name: Emovi Inc
• Labeler DUNS: 247640605
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2022-03-23
• Public Version: 2
• Public Version Date: 2023-03-10
• Public Version Status: Update
• Public Device Record Key: 6c0e25be-c6bb-4e18-ab7d-fd1633eb9b6a

Device Characteristics

• Single Use: No
• Prescription Use (Rx): Yes
• 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: Yes
• Has Lot/Batch Number: No
• Has Manufacturing Date: Yes
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
LXJ	Interactive Rehabilitation Exercise Devices	Physical Medicine	890.5360	2

GMDN Terms

Code	Name	Definition	Implantable	Status
35757	Gait analysis system	An assembly of mains electricity (AC-powered) devices and instruments intended to be used to study walking or running patterns. The device uses a platform/mat that measures ground reaction forces or relative pressures (e.g., foot pressure mapping), and/or uses cameras to determine knee, ankle, and hip joint movements and to measure forces and torques. It can be used to diagnose problems related to walking or running and to help plan corrective actions.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00627843933236	GS1

Premarket Submissions

Submission Number	Supplement Number
K091000	000