meddevicedb.com FDA Device Reference

PREP AND OPERATING STAND

K905564 Class I Traditional
Decision Date
1991-02-21
Sponsor / Applicant
Mcconnell Orthopedic

Technical Specification

510(k) Submission ID K905564
Product Code FWZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4950
Decision Date 1991-02-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PREP AND OPERATING STAND received FDA 510(k) clearance under submission number K905564, sponsored by Mcconnell Orthopedic. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1991-02-21.

Classification & Regulation

This clearance is catalogued under FDA product code FWZ and 21 CFR 878.4950, within the General, Plastic Surgery review panel as a Class I device.