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MENTOR RAPID-SPAN (TM) TISSUE EXPANDER

K883303 Class I Traditional
Decision Date
1988-08-26
Sponsor / Applicant
Mentor Corp.

Technical Specification

510(k) Submission ID K883303
Product Code FZW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1988-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MENTOR RAPID-SPAN (TM) TISSUE EXPANDER received FDA 510(k) clearance under submission number K883303, sponsored by Mentor 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 1988-08-26.

Classification & Regulation

This clearance is catalogued under FDA product code FZW and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.