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FDA 510(k)

Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules

K-Number: K243706 · 2025-01-17

ApplicantMedtronic Sofamor Danek, Inc.
Decision Date2025-01-17
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Sofamor Danek, Inc.. It received FDA 510(k) clearance on 2025-01-17 under 510(k) number K243706. 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 Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules?

Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules is a medical device that received FDA 510(k) clearance on 2025-01-17. The listed applicant is Medtronic Sofamor Danek, Inc.. The 510(k) number is K243706.

When did Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules receive FDA 510(k) clearance?

Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules received FDA 510(k) clearance on 2025-01-17, under 510(k) number K243706.

Who is the listed applicant for Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules?

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

What is the FDA product code for Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules?

The FDA product code for Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules is 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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