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HEAD FIXATION ARC AND TABLE BASE

K091439 Class II Traditional
Decision Date
2009-08-25
Sponsor / Applicant
Surgivision, Inc.

Technical Specification

510(k) Submission ID K091439
Product Code HBL
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4460
Decision Date 2009-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEAD FIXATION ARC AND TABLE BASE received FDA 510(k) clearance under submission number K091439, sponsored by Surgivision, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2009-08-25.

Classification & Regulation

This clearance is catalogued under FDA product code HBL and 21 CFR 882.4460, within the Neurology review panel as a Class II device.