meddevicedb.com FDA Device Reference

ONCOLOGY SALVAGE SYSTEM

K002757 Class II Traditional
Decision Date
2000-11-24
Sponsor / Applicant
Biomet, Inc.

Technical Specification

510(k) Submission ID K002757
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 2000-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ONCOLOGY SALVAGE SYSTEM received FDA 510(k) clearance under submission number K002757, sponsored by Biomet, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2000-11-24.

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.