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FDA 510(k)

WAGNER CONE PROSTHESIS

K-Number: K032380 · 2003-09-22

ApplicantCenterpulse Orthopedics, Inc.
Decision Date2003-09-22
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WAGNER CONE PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Centerpulse Orthopedics, Inc.. It received FDA 510(k) clearance on 2003-09-22 under 510(k) number K032380. 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 CONE PROSTHESIS?

WAGNER CONE PROSTHESIS is a medical device that received FDA 510(k) clearance on 2003-09-22. The listed applicant is Centerpulse Orthopedics, Inc.. The 510(k) number is K032380.

When did WAGNER CONE PROSTHESIS receive FDA 510(k) clearance?

WAGNER CONE PROSTHESIS received FDA 510(k) clearance on 2003-09-22, under 510(k) number K032380.

Who is the listed applicant for WAGNER CONE PROSTHESIS?

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

What is the FDA product code for WAGNER CONE PROSTHESIS?

The FDA product code for WAGNER CONE PROSTHESIS is LZO.

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Related Devices (Code: LZO)

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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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