meddevicedb.com FDA Device Reference

Bambino 3, S3 and S3 Swing, U3 and U3 Light, X

K220698 Class I Traditional
Decision Date
2023-02-16
Sponsor / Applicant
Panthera AB

Technical Specification

510(k) Submission ID K220698
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2023-02-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Bambino 3, S3 and S3 Swing, U3 and U3 Light, X received FDA 510(k) clearance under submission number K220698, sponsored by Panthera AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2023-02-16.

Classification & Regulation

This clearance is catalogued under FDA product code IOR and 21 CFR 890.3850, within the Physical Medicine review panel as a Class I device.