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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 the device name listed in this FDA 510(k) record. The listed applicant is Stryker. It received FDA 510(k) clearance on 2019-06-28 under 510(k) 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. The listed applicant is Stryker. The 510(k) number is K190696.

When did Stryker Surgeon iD Mandible Recon Plate receive FDA 510(k) clearance?

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

Who is the listed applicant for Stryker Surgeon iD Mandible Recon Plate?

The FDA 510(k) record lists Stryker as the applicant. This does not by itself establish the device manufacturer.

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.

Related Clinical Trials

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Related Devices (Code: JEY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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