meddevicedb.com FDA Device Reference

DETACHATIP III PLUS INSTRUMENT TRAY MODEL 3-4343

K123175 Class II Abbreviated
Decision Date
2013-02-21
Sponsor / Applicant
Conmed Corporation

Technical Specification

510(k) Submission ID K123175
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2013-02-21
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DETACHATIP III PLUS INSTRUMENT TRAY MODEL 3-4343 received FDA 510(k) clearance under submission number K123175, sponsored by Conmed Corporation. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2013-02-21.

Classification & Regulation

This clearance is catalogued under FDA product code KCT and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.