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FDA 510(k)

Stryker Surgeon iD Mandible Recon Plate

K-Number: K190696 · 2019-06-28

ApplicantStryker
Decision Date2019-06-28
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Stryker Surgeon iD Mandible Recon Plate is a medical device manufactured by Stryker. It received FDA 510(k) clearance on 2019-06-28 under approval number K190696. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Stryker Surgeon iD Mandible Recon Plate?

Stryker Surgeon iD Mandible Recon Plate is a medical device that received FDA 510(k) clearance on 2019-06-28. It is manufactured by Stryker. The 510(k) number is K190696.

When was Stryker Surgeon iD Mandible Recon Plate approved by the FDA?

Stryker Surgeon iD Mandible Recon Plate received FDA 510(k) clearance on 2019-06-28, under approval number K190696.

What company makes Stryker Surgeon iD Mandible Recon Plate?

Stryker Surgeon iD Mandible Recon Plate is manufactured by Stryker.

What is the FDA product code for Stryker Surgeon iD Mandible Recon Plate?

The FDA product code for Stryker Surgeon iD Mandible Recon Plate is JEY.

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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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