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FDA 510(k)

Mazor X

K-Number: K163221 · 2017-04-04

ApplicantMazor Robotics , Ltd.
Decision Date2017-04-04
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Mazor X is the device name listed in this FDA 510(k) record. The listed applicant is Mazor Robotics , Ltd.. It received FDA 510(k) clearance on 2017-04-04 under 510(k) number K163221. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Mazor X?

Mazor X is a medical device that received FDA 510(k) clearance on 2017-04-04. The listed applicant is Mazor Robotics , Ltd.. The 510(k) number is K163221.

When did Mazor X receive FDA 510(k) clearance?

Mazor X received FDA 510(k) clearance on 2017-04-04, under 510(k) number K163221.

Who is the listed applicant for Mazor X?

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

What is the FDA product code for Mazor X?

The FDA product code for Mazor X is OLO.

Other records listing Mazor Robotics , Ltd. 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.

K251316Mazor X System / Mazor X Stealth EditionK230064Mazor X System (Mazor X Stealth Edition)K203005Mazor XK200935Mazor XK182077Mazor X System (Mazor X Stealth Edition)K180307Mazor X

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Related Devices (Code: OLO)

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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