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FDA 510(k)

Stryker PEEK Customized Cranial Implant Kit

K-Number: K203055 · 2021-02-09

ApplicantStryker
Decision Date2021-02-09
Product CodeGWO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Stryker PEEK Customized Cranial Implant Kit is a medical device manufactured by Stryker. It received FDA 510(k) clearance on 2021-02-09 under approval number K203055. The device is classified under product code GWO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Stryker PEEK Customized Cranial Implant Kit?

Stryker PEEK Customized Cranial Implant Kit is a medical device that received FDA 510(k) clearance on 2021-02-09. It is manufactured by Stryker. The 510(k) number is K203055.

When was Stryker PEEK Customized Cranial Implant Kit approved by the FDA?

Stryker PEEK Customized Cranial Implant Kit received FDA 510(k) clearance on 2021-02-09, under approval number K203055.

What company makes Stryker PEEK Customized Cranial Implant Kit?

Stryker PEEK Customized Cranial Implant Kit is manufactured by Stryker.

What is the FDA product code for Stryker PEEK Customized Cranial Implant Kit?

The FDA product code for Stryker PEEK Customized Cranial Implant Kit is GWO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.