meddevicedb.com FDA Device Reference

C-O-T SET (CANNULA, OBTURATOR AND TROCAR) #TM-1360

K873650 Class II Traditional
Decision Date
1987-11-02
Sponsor / Applicant
Arthropedics, Inc.

Technical Specification

510(k) Submission ID K873650
Product Code HRX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1100
Decision Date 1987-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

C-O-T SET (CANNULA, OBTURATOR AND TROCAR) #TM-1360 received FDA 510(k) clearance under submission number K873650, sponsored by Arthropedics, 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 1987-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code HRX and 21 CFR 888.1100, within the Orthopedic review panel as a Class II device.