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FDA 510(k)

DUAL LOCK HIP STEM

K-Number: K980794 · 1998-05-20

ApplicantDepuy, Inc.
Decision Date1998-05-20
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DUAL LOCK HIP STEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1998-05-20 under 510(k) number K980794. 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 DUAL LOCK HIP STEM?

DUAL LOCK HIP STEM is a medical device that received FDA 510(k) clearance on 1998-05-20. The listed applicant is Depuy, Inc.. The 510(k) number is K980794.

When did DUAL LOCK HIP STEM receive FDA 510(k) clearance?

DUAL LOCK HIP STEM received FDA 510(k) clearance on 1998-05-20, under 510(k) number K980794.

Who is the listed applicant for DUAL LOCK HIP STEM?

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 DUAL LOCK HIP STEM?

The FDA product code for DUAL LOCK HIP STEM is JDI.

Other records listing Depuy, Inc. as applicant

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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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