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FDA 510(k)

TRIATHLON PRESS-FIT TOTAL KNEE SYSTEM

K-Number: K051380 · 2005-08-30

Decision Date2005-08-30
Product CodeMBH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRIATHLON PRESS-FIT TOTAL KNEE SYSTEM 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 2005-08-30 under 510(k) number K051380. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIATHLON PRESS-FIT TOTAL KNEE SYSTEM?

TRIATHLON PRESS-FIT TOTAL KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 2005-08-30. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K051380.

When did TRIATHLON PRESS-FIT TOTAL KNEE SYSTEM receive FDA 510(k) clearance?

TRIATHLON PRESS-FIT TOTAL KNEE SYSTEM received FDA 510(k) clearance on 2005-08-30, under 510(k) number K051380.

Who is the listed applicant for TRIATHLON PRESS-FIT TOTAL KNEE SYSTEM?

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 TRIATHLON PRESS-FIT TOTAL KNEE SYSTEM?

The FDA product code for TRIATHLON PRESS-FIT TOTAL KNEE SYSTEM is MBH.

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.

Other records listing Howmedica Osteonics Corp. 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: MBH)

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.

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