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FDA 510(k)

Xia® 3 Spinal System, Stryker Spine Power Adaptor Instrument Accessory

K-Number: K170496 · 2017-05-16

Decision Date2017-05-16
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Xia® 3 Spinal System, Stryker Spine Power Adaptor Instrument Accessory is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corporation. It received FDA 510(k) clearance on 2017-05-16 under 510(k) number K170496. 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 Xia® 3 Spinal System, Stryker Spine Power Adaptor Instrument Accessory?

Xia® 3 Spinal System, Stryker Spine Power Adaptor Instrument Accessory is a medical device that received FDA 510(k) clearance on 2017-05-16. The listed applicant is Stryker Corporation. The 510(k) number is K170496.

When did Xia® 3 Spinal System, Stryker Spine Power Adaptor Instrument Accessory receive FDA 510(k) clearance?

Xia® 3 Spinal System, Stryker Spine Power Adaptor Instrument Accessory received FDA 510(k) clearance on 2017-05-16, under 510(k) number K170496.

Who is the listed applicant for Xia® 3 Spinal System, Stryker Spine Power Adaptor Instrument Accessory?

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

What is the FDA product code for Xia® 3 Spinal System, Stryker Spine Power Adaptor Instrument Accessory?

The FDA product code for Xia® 3 Spinal System, Stryker Spine Power Adaptor Instrument Accessory is NKB.

Related Clinical Trials

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.

Other records listing Stryker Corporation as applicant

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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Related Devices (Code: NKB)

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.

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.