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CAST MATERIAL (WICKET STOCKINETTE)

K760003 Class I Traditional
Decision Date
1976-07-26
Sponsor / Applicant
Zimmer, Inc.

Technical Specification

510(k) Submission ID K760003
Product Code ITG
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3025
Decision Date 1976-07-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAST MATERIAL (WICKET STOCKINETTE) received FDA 510(k) clearance under submission number K760003, sponsored by Zimmer, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1976-07-26.

Classification & Regulation

This clearance is catalogued under FDA product code ITG and 21 CFR 890.3025, within the Physical Medicine review panel as a Class I device.