meddevicedb.com FDA Device Reference

Triathlon PKR System

K203099 Class II Traditional
Decision Date
2020-10-27
Sponsor / Applicant
Howmedica Osteonics Corp. A.K.A. Stryker Orthopaedics

Technical Specification

510(k) Submission ID K203099
Product Code HSX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3520
Decision Date 2020-10-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Triathlon PKR System received FDA 510(k) clearance under submission number K203099, sponsored by Howmedica Osteonics Corp. A.K.A. Stryker Orthopaedics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2020-10-27.

Classification & Regulation

This clearance is catalogued under FDA product code HSX and 21 CFR 888.3520, within the Orthopedic review panel as a Class II device.