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FDA 510(k)

Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments

K-Number: K190172 · 2019-06-14

ApplicantStryker
Decision Date2019-06-14
Product CodeHBE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments is a medical device manufactured by Stryker. It received FDA 510(k) clearance on 2019-06-14 under approval number K190172. The device is classified under product code HBE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments?

Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments is a medical device that received FDA 510(k) clearance on 2019-06-14. It is manufactured by Stryker. The 510(k) number is K190172.

When was Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments approved by the FDA?

Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments received FDA 510(k) clearance on 2019-06-14, under approval number K190172.

What company makes Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments?

Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments is manufactured by Stryker.

What is the FDA product code for Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments?

The FDA product code for Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments is HBE.

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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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