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FDA 510(k)

PATELLAR COMPONENT FOR LUBINUS PATELLAR

K-Number: K800800 · 1980-04-21

ApplicantWaldemar Link GmbH & Co. KG
Decision Date1980-04-21
Product CodeHTG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PATELLAR COMPONENT FOR LUBINUS PATELLAR is the device name listed in this FDA 510(k) record. The listed applicant is Waldemar Link GmbH & Co. KG. It received FDA 510(k) clearance on 1980-04-21 under 510(k) number K800800. The device is classified under product code HTG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATELLAR COMPONENT FOR LUBINUS PATELLAR?

PATELLAR COMPONENT FOR LUBINUS PATELLAR is a medical device that received FDA 510(k) clearance on 1980-04-21. The listed applicant is Waldemar Link GmbH & Co. KG. The 510(k) number is K800800.

When did PATELLAR COMPONENT FOR LUBINUS PATELLAR receive FDA 510(k) clearance?

PATELLAR COMPONENT FOR LUBINUS PATELLAR received FDA 510(k) clearance on 1980-04-21, under 510(k) number K800800.

Who is the listed applicant for PATELLAR COMPONENT FOR LUBINUS PATELLAR?

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

What is the FDA product code for PATELLAR COMPONENT FOR LUBINUS PATELLAR?

The FDA product code for PATELLAR COMPONENT FOR LUBINUS PATELLAR is HTG.

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Other records listing Waldemar Link GmbH & Co. KG 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: HTG)

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.

K771708WORRELL PATELLADepuy, Inc.

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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