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FDA 510(k)

Montage- XT Settable, Resorbable Hemostatic Bone Putty

K-Number: K232998 · 2023-10-12

Decision Date2023-10-12
Product CodeMTJ
DecisionSubstantially Equivalent

Device Summary

Montage- XT Settable, Resorbable Hemostatic Bone Putty is a medical device manufactured by Orthocon, Inc.. It received FDA 510(k) clearance on 2023-10-12 under approval number K232998. The device is classified under product code MTJ. FDA Decision: Substantially Equivalent.

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.

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Related Devices (Code: MTJ)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.