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FDA 510(k)

LINK MP Monoblock Hip Prosthesis

K-Number: K183141 · 2019-02-08

Decision Date2019-02-08
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LINK MP Monoblock Hip Prosthesis 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 2019-02-08 under 510(k) number K183141. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINK MP Monoblock Hip Prosthesis?

LINK MP Monoblock Hip Prosthesis is a medical device that received FDA 510(k) clearance on 2019-02-08. The listed applicant is Waldemar Link GmbH & Co. KG. The 510(k) number is K183141.

When did LINK MP Monoblock Hip Prosthesis receive FDA 510(k) clearance?

LINK MP Monoblock Hip Prosthesis received FDA 510(k) clearance on 2019-02-08, under 510(k) number K183141.

Who is the listed applicant for LINK MP Monoblock Hip Prosthesis?

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 LINK MP Monoblock Hip Prosthesis?

The FDA product code for LINK MP Monoblock Hip Prosthesis is LZO.

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: LZO)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.