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FDA 510(k)

ACCOLADE TMZF PLUS HA 127 SIZE 0 HIP STEM

K-Number: K023102 · 2002-10-09

ApplicantHowmedica Osteonics Corp.
Decision Date2002-10-09
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACCOLADE TMZF PLUS HA 127 SIZE 0 HIP STEM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 2002-10-09 under 510(k) number K023102. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCOLADE TMZF PLUS HA 127 SIZE 0 HIP STEM?

ACCOLADE TMZF PLUS HA 127 SIZE 0 HIP STEM is a medical device that received FDA 510(k) clearance on 2002-10-09. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K023102.

When did ACCOLADE TMZF PLUS HA 127 SIZE 0 HIP STEM receive FDA 510(k) clearance?

ACCOLADE TMZF PLUS HA 127 SIZE 0 HIP STEM received FDA 510(k) clearance on 2002-10-09, under 510(k) number K023102.

Who is the listed applicant for ACCOLADE TMZF PLUS HA 127 SIZE 0 HIP STEM?

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

What is the FDA product code for ACCOLADE TMZF PLUS HA 127 SIZE 0 HIP STEM?

The FDA product code for ACCOLADE TMZF PLUS HA 127 SIZE 0 HIP STEM is MEH.

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Other records listing Howmedica Osteonics Corp. as applicant

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Related Devices (Code: MEH)

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.

K261576Icona Hip StemCorin, Ltd.K250375Allure Hip Stem and Intramedullary PlugsWaldemar Link GmbH & Co. KGK251166Mfinity Femoral SystemMedacta International S.A.K251052Trivicta® Hip StemOrtho Development Corp.K242315Resolve Modular Revision Hip StemUnited Orthopedic CorporationK243839Alteon® HA Femoral StemsExactech, 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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