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FDA 510(k)

Stryker MP, Mandible, HMMF and MMF AXS Screws

K-Number: K231599 · 2023-08-24

ApplicantStryker Leibinger GmbH & Co KG
Decision Date2023-08-24
Product CodeDZL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Stryker MP, Mandible, HMMF and MMF AXS Screws is a medical device manufactured by Stryker Leibinger GmbH & Co KG. It received FDA 510(k) clearance on 2023-08-24 under approval number K231599. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Stryker MP, Mandible, HMMF and MMF AXS Screws?

Stryker MP, Mandible, HMMF and MMF AXS Screws is a medical device that received FDA 510(k) clearance on 2023-08-24. It is manufactured by Stryker Leibinger GmbH & Co KG. The 510(k) number is K231599.

When was Stryker MP, Mandible, HMMF and MMF AXS Screws approved by the FDA?

Stryker MP, Mandible, HMMF and MMF AXS Screws received FDA 510(k) clearance on 2023-08-24, under approval number K231599.

What company makes Stryker MP, Mandible, HMMF and MMF AXS Screws?

Stryker MP, Mandible, HMMF and MMF AXS Screws is manufactured by Stryker Leibinger GmbH & Co KG.

What is the FDA product code for Stryker MP, Mandible, HMMF and MMF AXS Screws?

The FDA product code for Stryker MP, Mandible, HMMF and MMF AXS Screws is DZL.

Related Clinical Trials

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Related Devices (Code: DZL)

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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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