meddevicedb.com FDA Device Reference

C-S IMPACTOR

K890185 Class II Traditional
Decision Date
1989-04-06
Sponsor / Applicant
Orthopedic Systems, Inc.

Technical Specification

510(k) Submission ID K890185
Product Code LYP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3050
Decision Date 1989-04-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

C-S IMPACTOR received FDA 510(k) clearance under submission number K890185, sponsored by Orthopedic Systems, 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 1989-04-06.

Classification & Regulation

This clearance is catalogued under FDA product code LYP and 21 CFR 888.3050, within the Orthopedic review panel as a Class II device.