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FDA 510(k)

SPINEASSIST SYSTEM

K-Number: K073467 · 2008-05-23

Decision Date2008-05-23
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SPINEASSIST SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mazor Surgical Technologies , Ltd.. It received FDA 510(k) clearance on 2008-05-23 under 510(k) number K073467. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINEASSIST SYSTEM?

SPINEASSIST SYSTEM is a medical device that received FDA 510(k) clearance on 2008-05-23. The listed applicant is Mazor Surgical Technologies , Ltd.. The 510(k) number is K073467.

When did SPINEASSIST SYSTEM receive FDA 510(k) clearance?

SPINEASSIST SYSTEM received FDA 510(k) clearance on 2008-05-23, under 510(k) number K073467.

Who is the listed applicant for SPINEASSIST SYSTEM?

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

What is the FDA product code for SPINEASSIST SYSTEM?

The FDA product code for SPINEASSIST SYSTEM is HAW.

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 Mazor Surgical Technologies , 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.

View all 7 devices →

Related Devices (Code: HAW)

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

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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