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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Orthocon, Inc.. It received FDA 510(k) clearance on 2024-11-18 under 510(k) 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. The listed applicant is Orthocon, Inc.. The 510(k) number is K243506.

When did Montage-XT Settable Bone Putty receive FDA 510(k) clearance?

Montage-XT Settable Bone Putty received FDA 510(k) clearance on 2024-11-18, under 510(k) number K243506.

Who is the listed applicant for Montage-XT Settable Bone Putty?

The FDA 510(k) record lists Orthocon, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Montage-XT Settable Bone Putty?

The FDA product code for Montage-XT Settable Bone Putty is MQV.

Other records listing Orthocon, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261265Permatage XT Settable Bone PuttyK261439Permatage Flowable, Settable Hemostatic Bone PasteK253447Montage Flowable Settable, Resorbable Bone Paste (Burr Hole Cover)K253732Permatage Flowable, Settable Bone PasteK253854MONTAGE XT Cranial CementK243526MONTAGE Settable, Resorbable Bone Putty MONTAGE-QS Settable, Resorbable Bone Putty MONTAGE Flowable Settable, Resorbable Bone Paste MONTAGE-XT Settable, Resorbable Hemostatic Bone Putty

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Related Devices (Code: MQV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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