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FDA 510(k)

Montage-QS Settable, Resorbable Bone Putty

K-Number: K231903 · 2023-08-25

ApplicantOrthocon, Inc.
Decision Date2023-08-25
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Montage-QS Settable, Resorbable Bone Putty is a medical device manufactured by Orthocon, Inc.. It received FDA 510(k) clearance on 2023-08-25 under approval number K231903. 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-QS Settable, Resorbable Bone Putty?

Montage-QS Settable, Resorbable Bone Putty is a medical device that received FDA 510(k) clearance on 2023-08-25. It is manufactured by Orthocon, Inc.. The 510(k) number is K231903.

When was Montage-QS Settable, Resorbable Bone Putty approved by the FDA?

Montage-QS Settable, Resorbable Bone Putty received FDA 510(k) clearance on 2023-08-25, under approval number K231903.

What company makes Montage-QS Settable, Resorbable Bone Putty?

Montage-QS Settable, Resorbable Bone Putty is manufactured by Orthocon, Inc..

What is the FDA product code for Montage-QS Settable, Resorbable Bone Putty?

The FDA product code for Montage-QS Settable, Resorbable Bone Putty is MQV.

Other Devices by Orthocon, Inc.

K153317HEMASORBPLUS Resorbable Hemostatic Bone Putty K191140MONTAGE-QS Settable, Resorbable Hemostatic Bone K193052HBP6 Settable, Resorbable Hemostatic Bone Paste K202363HBP7 Settable Hemostatic Bone Putty K220315MONTAGE-XT Settable, Resorbable Hemostatic Bone Putty K231475MONTAGE-QS Settable, Resorbable Bone Putty

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Related Devices (Code: MQV)

K160566Cerasorb Ortho FoamCurasan AG K160446MCP Bone PuttyBiostructures, LLC K161351NanoBone SBX PuttyArtoss GmbH K161447HydroSet XTOrthovita, Inc. K152077MaxiGenHans Biomed Corp. K151271BellaFuseHans Biomed Corp.

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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