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FDA 510(k)

ORTHO DEVELOPMENT CERAMIC FEMORAL HEADS

K-Number: K060577 · 2006-04-28

ApplicantOrtho Development Corp.
Decision Date2006-04-28
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ORTHO DEVELOPMENT CERAMIC FEMORAL HEADS is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Development Corp.. It received FDA 510(k) clearance on 2006-04-28 under 510(k) number K060577. 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 ORTHO DEVELOPMENT CERAMIC FEMORAL HEADS?

ORTHO DEVELOPMENT CERAMIC FEMORAL HEADS is a medical device that received FDA 510(k) clearance on 2006-04-28. The listed applicant is Ortho Development Corp.. The 510(k) number is K060577.

When did ORTHO DEVELOPMENT CERAMIC FEMORAL HEADS receive FDA 510(k) clearance?

ORTHO DEVELOPMENT CERAMIC FEMORAL HEADS received FDA 510(k) clearance on 2006-04-28, under 510(k) number K060577.

Who is the listed applicant for ORTHO DEVELOPMENT CERAMIC FEMORAL HEADS?

The FDA 510(k) record lists Ortho Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORTHO DEVELOPMENT CERAMIC FEMORAL HEADS?

The FDA product code for ORTHO DEVELOPMENT CERAMIC FEMORAL HEADS 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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