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FDA 510(k)

Montage Flowable Settable, Resorbable Bone Paste

K-Number: K231270 · 2023-09-01

ApplicantOrthocon, Inc.
Decision Date2023-09-01
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Montage Flowable Settable, Resorbable Bone Paste is a medical device manufactured by Orthocon, Inc.. It received FDA 510(k) clearance on 2023-09-01 under approval number K231270. 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 Flowable Settable, Resorbable Bone Paste?

Montage Flowable Settable, Resorbable Bone Paste is a medical device that received FDA 510(k) clearance on 2023-09-01. It is manufactured by Orthocon, Inc.. The 510(k) number is K231270.

When was Montage Flowable Settable, Resorbable Bone Paste approved by the FDA?

Montage Flowable Settable, Resorbable Bone Paste received FDA 510(k) clearance on 2023-09-01, under approval number K231270.

What company makes Montage Flowable Settable, Resorbable Bone Paste?

Montage Flowable Settable, Resorbable Bone Paste is manufactured by Orthocon, Inc..

What is the FDA product code for Montage Flowable Settable, Resorbable Bone Paste?

The FDA product code for Montage Flowable Settable, Resorbable Bone Paste is MQV.

Other Devices by Orthocon, Inc.

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Related Devices (Code: MQV)

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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.

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