meddevicedb.com FDA Device Reference

COMPUTER ASSIST STEREOTACTIC SURG SYST, MODIFIED

K911750 Class II Traditional
Decision Date
1991-10-15
Sponsor / Applicant
Medical Instrumentation & Diagnostics Corp.(Midco)

Technical Specification

510(k) Submission ID K911750
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 1991-10-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPUTER ASSIST STEREOTACTIC SURG SYST, MODIFIED received FDA 510(k) clearance under submission number K911750, sponsored by Medical Instrumentation & Diagnostics Corp.(Midco). The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1991-10-15.

Classification & Regulation

This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.