Montage Settable Bone Putty
K-Number: K242050 · 2024-07-29
ApplicantOrthocon, Inc.
Decision Date2024-07-29
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Montage Settable Bone Putty is a medical device manufactured by Orthocon, Inc.. It received FDA 510(k) clearance on 2024-07-29 under approval number K242050. 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 Settable Bone Putty?
Montage Settable Bone Putty is a medical device that received FDA 510(k) clearance on 2024-07-29. It is manufactured by Orthocon, Inc.. The 510(k) number is K242050.
When was Montage Settable Bone Putty approved by the FDA?
Montage Settable Bone Putty received FDA 510(k) clearance on 2024-07-29, under approval number K242050.
What company makes Montage Settable Bone Putty?
Montage Settable Bone Putty is manufactured by Orthocon, Inc..
What is the FDA product code for Montage Settable Bone Putty?
The FDA product code for Montage Settable Bone Putty is MQV.
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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.