FDA 510(k)

TEZO TITANIUM CAGE FAMILY

K-Number: K122957 · 2013-06-21

Decision Date2013-06-21

Product CodeMAX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

TEZO TITANIUM CAGE FAMILY is the device name listed in this FDA 510(k) record. The listed applicant is Ulrich GmbH & Co. KG. It received FDA 510(k) clearance on 2013-06-21 under 510(k) number K122957. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEZO TITANIUM CAGE FAMILY?

TEZO TITANIUM CAGE FAMILY is a medical device that received FDA 510(k) clearance on 2013-06-21. The listed applicant is Ulrich GmbH & Co. KG. The 510(k) number is K122957.

When did TEZO TITANIUM CAGE FAMILY receive FDA 510(k) clearance?

TEZO TITANIUM CAGE FAMILY received FDA 510(k) clearance on 2013-06-21, under 510(k) number K122957.

Who is the listed applicant for TEZO TITANIUM CAGE FAMILY?

The FDA 510(k) record lists Ulrich GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEZO TITANIUM CAGE FAMILY?

The FDA product code for TEZO TITANIUM CAGE FAMILY is MAX.

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Other records listing Ulrich GmbH & Co. KG as applicant

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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.