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FDA 510(k)

TIBIAL PLATEU

K-Number: K780284 · 1978-03-15

ApplicantDepuy, Inc.
Decision Date1978-03-15
Product CodeMBV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TIBIAL PLATEU is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1978-03-15 under 510(k) number K780284. The device is classified under product code MBV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIBIAL PLATEU?

TIBIAL PLATEU is a medical device that received FDA 510(k) clearance on 1978-03-15. The listed applicant is Depuy, Inc.. The 510(k) number is K780284.

When did TIBIAL PLATEU receive FDA 510(k) clearance?

TIBIAL PLATEU received FDA 510(k) clearance on 1978-03-15, under 510(k) number K780284.

Who is the listed applicant for TIBIAL PLATEU?

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

What is the FDA product code for TIBIAL PLATEU?

The FDA product code for TIBIAL PLATEU is MBV.

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 Depuy, 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: MBV)

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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