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IMSI/METRIPOND HAND OPERATING TABLE

K830339 Class I Traditional
Decision Date
1983-04-12
Sponsor / Applicant
Intl. Management Services, Inc.

Technical Specification

510(k) Submission ID K830339
Product Code FSE
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4950
Decision Date 1983-04-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMSI/METRIPOND HAND OPERATING TABLE received FDA 510(k) clearance under submission number K830339, sponsored by Intl. Management Services, 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 1983-04-12.

Classification & Regulation

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