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STRUNG NEURO SPONGE PATTIES-X-RAY-

K831914 Class I Traditional
Decision Date
1983-10-31
Sponsor / Applicant
Ormed Mfg., Inc.

Technical Specification

510(k) Submission ID K831914
Product Code GDY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4450
Decision Date 1983-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STRUNG NEURO SPONGE PATTIES-X-RAY- received FDA 510(k) clearance under submission number K831914, sponsored by Ormed Mfg., 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 1983-10-31.

Classification & Regulation

This clearance is catalogued under FDA product code GDY and 21 CFR 878.4450, within the General, Plastic Surgery review panel as a Class I device.