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FDA 510(k)

WAGNER SL REVISION STEM LATERAL

K-Number: K043356 · 2005-04-18

ApplicantZimmer Austin, Inc.
Decision Date2005-04-18
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WAGNER SL REVISION STEM LATERAL is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Austin, Inc.. It received FDA 510(k) clearance on 2005-04-18 under 510(k) number K043356. 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 WAGNER SL REVISION STEM LATERAL?

WAGNER SL REVISION STEM LATERAL is a medical device that received FDA 510(k) clearance on 2005-04-18. The listed applicant is Zimmer Austin, Inc.. The 510(k) number is K043356.

When did WAGNER SL REVISION STEM LATERAL receive FDA 510(k) clearance?

WAGNER SL REVISION STEM LATERAL received FDA 510(k) clearance on 2005-04-18, under 510(k) number K043356.

Who is the listed applicant for WAGNER SL REVISION STEM LATERAL?

The FDA 510(k) record lists Zimmer Austin, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WAGNER SL REVISION STEM LATERAL?

The FDA product code for WAGNER SL REVISION STEM LATERAL is LZO.

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.

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Other records listing Zimmer Austin, Inc. 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.

K042249CLS SPOTORNO STEM

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.

K260173M-Vizion Femoral Revision System ExtensionMedacta International S.A.K253948Momentum Acetabular Cup SystemUnited Orthopedic CorporationK261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbH

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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