meddevicedb.com FDA Device Reference

ORTHOCON ABSORBABLE HEMOSTATIC BONE PUTTY

K122156 Traditional
Decision Date
2013-01-28
Sponsor / Applicant
Orthocon, Inc.

Technical Specification

510(k) Submission ID K122156
Product Code MTJ
Medical Specialty / Panel Unknown
Decision Date 2013-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHOCON ABSORBABLE HEMOSTATIC BONE PUTTY received FDA 510(k) clearance under submission number K122156, sponsored by Orthocon, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Unknown review panel. The statutory decision date of record is 2013-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code MTJ , within the Unknown review panel as a device.