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FDA 510(k)

TITANIUM HIP 1019

K-Number: K843909 · 1984-11-15

ApplicantDepuy, Inc.
Decision Date1984-11-15
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITANIUM HIP 1019 is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1984-11-15 under 510(k) number K843909. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITANIUM HIP 1019?

TITANIUM HIP 1019 is a medical device that received FDA 510(k) clearance on 1984-11-15. The listed applicant is Depuy, Inc.. The 510(k) number is K843909.

When did TITANIUM HIP 1019 receive FDA 510(k) clearance?

TITANIUM HIP 1019 received FDA 510(k) clearance on 1984-11-15, under 510(k) number K843909.

Who is the listed applicant for TITANIUM HIP 1019?

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 TITANIUM HIP 1019?

The FDA product code for TITANIUM HIP 1019 is JDI.

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Related Devices (Code: JDI)

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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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