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FDA 510(k)

PLATFORM TCCK TOTAL KNEE

K-Number: K790762 · 1979-05-14

ApplicantBiomet, Inc.
Decision Date1979-05-14
Product CodeHRY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PLATFORM TCCK TOTAL KNEE is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1979-05-14 under 510(k) number K790762. The device is classified under product code HRY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLATFORM TCCK TOTAL KNEE?

PLATFORM TCCK TOTAL KNEE is a medical device that received FDA 510(k) clearance on 1979-05-14. The listed applicant is Biomet, Inc.. The 510(k) number is K790762.

When did PLATFORM TCCK TOTAL KNEE receive FDA 510(k) clearance?

PLATFORM TCCK TOTAL KNEE received FDA 510(k) clearance on 1979-05-14, under 510(k) number K790762.

Who is the listed applicant for PLATFORM TCCK TOTAL KNEE?

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

What is the FDA product code for PLATFORM TCCK TOTAL KNEE?

The FDA product code for PLATFORM TCCK TOTAL KNEE is HRY.

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 Biomet, 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.

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Related Devices (Code: HRY)

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

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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