meddevicedb.com FDA Device Reference

Small Bone Phantom® Intramedullary Nail System; TTC Phantom® Intramedullary Nail System

K182307 Class II Traditional
Decision Date
2019-01-14
Sponsor / Applicant
Paragon 28, Inc.

Technical Specification

510(k) Submission ID K182307
Product Code HSB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3020
Decision Date 2019-01-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Small Bone Phantom® Intramedullary Nail System; TTC Phantom® Intramedullary Nail System received FDA 510(k) clearance under submission number K182307, sponsored by Paragon 28, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2019-01-14.

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.