meddevicedb.com FDA Device Reference

Permatage Flowable, Settable Hemostatic Bone Paste

K261439 Traditional
Decision Date
2026-06-03
Sponsor / Applicant
Orthocon, Inc.

Technical Specification

510(k) Submission ID K261439
Product Code MTJ
Medical Specialty / Panel Unknown
Decision Date 2026-06-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Permatage Flowable, Settable Hemostatic Bone Paste received FDA 510(k) clearance under submission number K261439, 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 2026-06-03.

Classification & Regulation

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