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FDA 510(k)

DTT SYSTEM

K-Number: K790404 · 1979-03-21

ApplicantDepuy, Inc.
Decision Date1979-03-21
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DTT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1979-03-21 under 510(k) number K790404. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DTT SYSTEM?

DTT SYSTEM is a medical device that received FDA 510(k) clearance on 1979-03-21. The listed applicant is Depuy, Inc.. The 510(k) number is K790404.

When did DTT SYSTEM receive FDA 510(k) clearance?

DTT SYSTEM received FDA 510(k) clearance on 1979-03-21, under 510(k) number K790404.

Who is the listed applicant for DTT SYSTEM?

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 DTT SYSTEM?

The FDA product code for DTT SYSTEM is KWQ.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: KWQ)

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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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