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KOBOLD SURE-GUIDE VAGINAL CYLINDER SET, STUMP VAGINAL CYLINDER SET, MIAMI CYLINDER SET

K123941 Class II Traditional
Decision Date
2013-04-30
Sponsor / Applicant
Spencer Fillmore

Technical Specification

510(k) Submission ID K123941
Product Code JAQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5700
Decision Date 2013-04-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KOBOLD SURE-GUIDE VAGINAL CYLINDER SET, STUMP VAGINAL CYLINDER SET, MIAMI CYLINDER SET received FDA 510(k) clearance under submission number K123941, sponsored by Spencer Fillmore. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2013-04-30.

Classification & Regulation

This clearance is catalogued under FDA product code JAQ and 21 CFR 892.5700, within the Radiology review panel as a Class II device.