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MODELS HRS-63-8 AND HRS-127-8 SHOULDER ARRAY COILS

K053017 Class II Special
Decision Date
2005-11-16
Sponsor / Applicant
Invivo Corporation

Technical Specification

510(k) Submission ID K053017
Product Code MOS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2005-11-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODELS HRS-63-8 AND HRS-127-8 SHOULDER ARRAY COILS received FDA 510(k) clearance under submission number K053017, sponsored by Invivo Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-11-16.

Classification & Regulation

This clearance is catalogued under FDA product code MOS and 21 CFR 892.1000, within the Radiology review panel as a Class II device.