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FDA 510(k)

GOLDEN GATE ANTERIOR PLATE SYSTEM

K-Number: K101353 · 2011-02-04

ApplicantUlrich GmbH & Co. KG
Decision Date2011-02-04
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GOLDEN GATE ANTERIOR PLATE SYSTEM 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 2011-02-04 under 510(k) number K101353. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOLDEN GATE ANTERIOR PLATE SYSTEM?

GOLDEN GATE ANTERIOR PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2011-02-04. The listed applicant is Ulrich GmbH & Co. KG. The 510(k) number is K101353.

When did GOLDEN GATE ANTERIOR PLATE SYSTEM receive FDA 510(k) clearance?

GOLDEN GATE ANTERIOR PLATE SYSTEM received FDA 510(k) clearance on 2011-02-04, under 510(k) number K101353.

Who is the listed applicant for GOLDEN GATE ANTERIOR PLATE SYSTEM?

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 GOLDEN GATE ANTERIOR PLATE SYSTEM?

The FDA product code for GOLDEN GATE ANTERIOR PLATE SYSTEM is KWQ.

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Other records listing Ulrich GmbH & Co. KG as applicant

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Related Devices (Code: KWQ)

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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