meddevicedb.com FDA Device Reference

CONTOUR NECKLIFT THREADS

K050247 Class II Traditional
Decision Date
2005-03-04
Sponsor / Applicant
Surgical Specialties Corp

Technical Specification

510(k) Submission ID K050247
Product Code GAW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5010
Decision Date 2005-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONTOUR NECKLIFT THREADS received FDA 510(k) clearance under submission number K050247, sponsored by Surgical Specialties Corp. 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 2005-03-04.

Classification & Regulation

This clearance is catalogued under FDA product code GAW and 21 CFR 878.5010, within the General, Plastic Surgery review panel as a Class II device.