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FDA 510(k)

DePuy Synthes MatrixSTERNUM Fixation System

K-Number: K233967 · 2024-05-09

ApplicantSynthes GmbH
Decision Date2024-05-09
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DePuy Synthes MatrixSTERNUM Fixation System is a medical device manufactured by Synthes GmbH. It received FDA 510(k) clearance on 2024-05-09 under approval number K233967. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DePuy Synthes MatrixSTERNUM Fixation System?

DePuy Synthes MatrixSTERNUM Fixation System is a medical device that received FDA 510(k) clearance on 2024-05-09. It is manufactured by Synthes GmbH. The 510(k) number is K233967.

When was DePuy Synthes MatrixSTERNUM Fixation System approved by the FDA?

DePuy Synthes MatrixSTERNUM Fixation System received FDA 510(k) clearance on 2024-05-09, under approval number K233967.

What company makes DePuy Synthes MatrixSTERNUM Fixation System?

DePuy Synthes MatrixSTERNUM Fixation System is manufactured by Synthes GmbH.

What is the FDA product code for DePuy Synthes MatrixSTERNUM Fixation System?

The FDA product code for DePuy Synthes MatrixSTERNUM Fixation System is HRS.

Related Clinical Trials

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Other Devices by Synthes GmbH

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Related Devices (Code: HRS)

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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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