meddevicedb.com FDA Device Reference

ELEOS Limb Salvage System with BioGrip

K203815 Class II Traditional
Decision Date
2021-06-09
Sponsor / Applicant
Onkos Surgical

Technical Specification

510(k) Submission ID K203815
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 2021-06-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELEOS Limb Salvage System with BioGrip received FDA 510(k) clearance under submission number K203815, sponsored by Onkos Surgical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2021-06-09.

Classification & Regulation

This clearance is catalogued under FDA product code JDI and 21 CFR 888.3350, within the Orthopedic review panel as a Class II device.