Montage-XT Settable Bone Putty
K-Number: K243506 · 2024-11-18
ApplicantOrthocon, Inc.
Decision Date2024-11-18
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Montage-XT Settable Bone Putty is a medical device manufactured by Orthocon, Inc.. It received FDA 510(k) clearance on 2024-11-18 under approval number K243506. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Montage-XT Settable Bone Putty?
Montage-XT Settable Bone Putty is a medical device that received FDA 510(k) clearance on 2024-11-18. It is manufactured by Orthocon, Inc.. The 510(k) number is K243506.
When was Montage-XT Settable Bone Putty approved by the FDA?
Montage-XT Settable Bone Putty received FDA 510(k) clearance on 2024-11-18, under approval number K243506.
What company makes Montage-XT Settable Bone Putty?
Montage-XT Settable Bone Putty is manufactured by Orthocon, Inc..
What is the FDA product code for Montage-XT Settable Bone Putty?
The FDA product code for Montage-XT Settable Bone Putty is MQV.
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K202363HBP7 Settable Hemostatic Bone Putty
K220315MONTAGE-XT Settable, Resorbable Hemostatic Bone Putty
K231475MONTAGE-QS Settable, Resorbable Bone Putty
Related Devices (Code: MQV)
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.