meddevicedb.com FDA Device Reference

OPTETRAK LOGIC PS 17MM & 19MM THICK INSERTS, OPTETRAK LOGIC PSC 17MM & 19MM THICK INSERTS

K132161 Class II Traditional
Decision Date
2013-10-11
Sponsor / Applicant
Exactech, Inc.

Technical Specification

510(k) Submission ID K132161
Product Code JWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2013-10-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPTETRAK LOGIC PS 17MM & 19MM THICK INSERTS, OPTETRAK LOGIC PSC 17MM & 19MM THICK INSERTS received FDA 510(k) clearance under submission number K132161, sponsored by Exactech, 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 2013-10-11.

Classification & Regulation

This clearance is catalogued under FDA product code JWH and 21 CFR 888.3560, within the Orthopedic review panel as a Class II device.