Decision Date2020-04-23
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Stryker Xia 3 Power Adaptor is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Spine. It received FDA 510(k) clearance on 2020-04-23 under 510(k) number K200666. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Stryker Xia 3 Power Adaptor?
Stryker Xia 3 Power Adaptor is a medical device that received FDA 510(k) clearance on 2020-04-23. The listed applicant is Stryker Spine. The 510(k) number is K200666.
When did Stryker Xia 3 Power Adaptor receive FDA 510(k) clearance?
Stryker Xia 3 Power Adaptor received FDA 510(k) clearance on 2020-04-23, under 510(k) number K200666.
Who is the listed applicant for Stryker Xia 3 Power Adaptor?
The FDA 510(k) record lists Stryker Spine as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stryker Xia 3 Power Adaptor?
The FDA product code for Stryker Xia 3 Power Adaptor is NKB.
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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.