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Signature ONE System

K200615 Class II Traditional
Decision Date
2020-06-05
Sponsor / Applicant
Orthosoft Inc (D/B/A Zimmer Cas)

Technical Specification

510(k) Submission ID K200615
Product Code QHE
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 2020-06-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Signature ONE System received FDA 510(k) clearance under submission number K200615, sponsored by Orthosoft Inc (D/B/A Zimmer Cas). The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2020-06-05.

Classification & Regulation

This clearance is catalogued under FDA product code QHE and 21 CFR 888.3660, within the Orthopedic review panel as a Class II device.