meddevicedb.com FDA Device Reference

PREVIEW SURGERY PLANNING SOFTWARE

K953616 Class II Traditional
Decision Date
1996-02-27
Sponsor / Applicant
Medical Media Systems

Technical Specification

510(k) Submission ID K953616
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 1996-02-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PREVIEW SURGERY PLANNING SOFTWARE received FDA 510(k) clearance under submission number K953616, sponsored by Medical Media Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1996-02-27.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.