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FDA 510(k)

AML TRI-LOCK REPLACEMENT LINER SYSTEM

K-Number: K943302 · 1994-10-14

ApplicantDepuy, Inc.
Decision Date1994-10-14
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AML TRI-LOCK REPLACEMENT LINER 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 1994-10-14 under 510(k) number K943302. 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 AML TRI-LOCK REPLACEMENT LINER SYSTEM?

AML TRI-LOCK REPLACEMENT LINER SYSTEM is a medical device that received FDA 510(k) clearance on 1994-10-14. The listed applicant is Depuy, Inc.. The 510(k) number is K943302.

When did AML TRI-LOCK REPLACEMENT LINER SYSTEM receive FDA 510(k) clearance?

AML TRI-LOCK REPLACEMENT LINER SYSTEM received FDA 510(k) clearance on 1994-10-14, under 510(k) number K943302.

Who is the listed applicant for AML TRI-LOCK REPLACEMENT LINER 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 AML TRI-LOCK REPLACEMENT LINER SYSTEM?

The FDA product code for AML TRI-LOCK REPLACEMENT LINER SYSTEM is JDI.

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Other records listing Depuy, Inc. as applicant

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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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