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PADLOCK CLIP-12

K120814 Class II Traditional
Decision Date
2012-09-06
Sponsor / Applicant
Aponos Medical Corp.

Technical Specification

510(k) Submission ID K120814
Product Code PKL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4400
Decision Date 2012-09-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PADLOCK CLIP-12 received FDA 510(k) clearance under submission number K120814, sponsored by Aponos Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2012-09-06.

Classification & Regulation

This clearance is catalogued under FDA product code PKL and 21 CFR 876.4400, within the Gastroenterology, Urology review panel as a Class II device.