meddevicedb.com FDA Device Reference

SURGASSIST RIGHT ANGLE LINEAR CUTTER DLU - 45MM, MODEL RALC45

K012809 Class II Traditional
Decision Date
2001-10-26
Sponsor / Applicant
Power Medical Interventions, Inc.

Technical Specification

510(k) Submission ID K012809
Product Code GDW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4750
Decision Date 2001-10-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGASSIST RIGHT ANGLE LINEAR CUTTER DLU - 45MM, MODEL RALC45 received FDA 510(k) clearance under submission number K012809, sponsored by Power Medical Interventions, Inc.. 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 2001-10-26.

Classification & Regulation

This clearance is catalogued under FDA product code GDW and 21 CFR 878.4750, within the General, Plastic Surgery review panel as a Class II device.