meddevicedb.com FDA Device Reference

Phantom® Hindfoot TTC/TC Nail System

K201227 Class II Special
Decision Date
2020-07-17
Sponsor / Applicant
Paragon 28, Inc.

Technical Specification

510(k) Submission ID K201227
Product Code HSB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3020
Decision Date 2020-07-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Phantom® Hindfoot TTC/TC Nail System received FDA 510(k) clearance under submission number K201227, sponsored by Paragon 28, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2020-07-17.

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.