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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 a medical device manufactured by Medtronic Sofamor Danek, Inc.. It received FDA 510(k) clearance on 2025-01-17 under approval 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. It is manufactured by Medtronic Sofamor Danek, Inc.. The 510(k) number is K243706.

When was Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules approved by the FDA?

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

What company makes Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules?

Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules is manufactured by Medtronic Sofamor Danek, Inc..

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.

Related Clinical Trials

NCT07546279 The Use of Two Bone Substitutes in Adjunct to EMD for the Treatment of One- and Two-wall Intrabony Defects. RECRUITING NCT07512336 A Randomized Intra-Patient Controlled Trial of MagnetOs™ Putty vs Autograft in Instrumented Posterolateral Spinal Fusion in Idiopathic Scoliosis Patients NOT_YET_RECRUITING

Other Devices by Medtronic Sofamor Danek, Inc.

K230716Robotic Graft Delivery Instruments K251193Grafton™ DBM; Grafton Plus™ DBM Paste; Magnifuse™ Bone Graft PMA P060018Prosthesis, intervertebral disc

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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