Montage- XT Settable, Resorbable Hemostatic Bone Putty
K-Number: K232998 · 2023-10-12
Device Summary
Frequently Asked Questions
What is the Montage- XT Settable, Resorbable Hemostatic Bone Putty?
Montage- XT Settable, Resorbable Hemostatic Bone Putty is a medical device that received FDA 510(k) clearance on 2023-10-12. It is manufactured by Orthocon, Inc.. The 510(k) number is K232998.
When was Montage- XT Settable, Resorbable Hemostatic Bone Putty approved by the FDA?
Montage- XT Settable, Resorbable Hemostatic Bone Putty received FDA 510(k) clearance on 2023-10-12, under approval number K232998.
What company makes Montage- XT Settable, Resorbable Hemostatic Bone Putty?
Montage- XT Settable, Resorbable Hemostatic Bone Putty is manufactured by Orthocon, Inc..
What is the FDA product code for Montage- XT Settable, Resorbable Hemostatic Bone Putty?
The FDA product code for Montage- XT Settable, Resorbable Hemostatic Bone Putty is MTJ.
Other Devices by Orthocon, Inc.
Related Devices (Code: MTJ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.