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FDA 510(k)

POROCOAT DUAL-LOCK TOTAL HIP SYSTEM

K-Number: K830004 · 1983-04-19

ApplicantDepuy, Inc.
Decision Date1983-04-19
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

POROCOAT DUAL-LOCK TOTAL HIP 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 1983-04-19 under 510(k) number K830004. 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 POROCOAT DUAL-LOCK TOTAL HIP SYSTEM?

POROCOAT DUAL-LOCK TOTAL HIP SYSTEM is a medical device that received FDA 510(k) clearance on 1983-04-19. The listed applicant is Depuy, Inc.. The 510(k) number is K830004.

When did POROCOAT DUAL-LOCK TOTAL HIP SYSTEM receive FDA 510(k) clearance?

POROCOAT DUAL-LOCK TOTAL HIP SYSTEM received FDA 510(k) clearance on 1983-04-19, under 510(k) number K830004.

Who is the listed applicant for POROCOAT DUAL-LOCK TOTAL HIP 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 POROCOAT DUAL-LOCK TOTAL HIP SYSTEM?

The FDA product code for POROCOAT DUAL-LOCK TOTAL HIP SYSTEM 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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