meddevicedb.com FDA Device Reference

Affixus(R) Natural Nail(R) System Humeral Nail

K200814 Class II Special
Decision Date
2020-04-28
Sponsor / Applicant
Zimmer GmbH

Technical Specification

510(k) Submission ID K200814
Product Code HSB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3020
Decision Date 2020-04-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Affixus(R) Natural Nail(R) System Humeral Nail received FDA 510(k) clearance under submission number K200814, sponsored by Zimmer GmbH. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2020-04-28.

Classification & Regulation

This clearance is catalogued under FDA product code HSB and 21 CFR 888.3020, within the Orthopedic review panel as a Class II device.