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FDA 510(k)

STANDARD POROCOAT MODIFIED MEDIAL ASPECT AML HIP

K-Number: K870699 · 1987-05-01

ApplicantDepuy, Inc.
Decision Date1987-05-01
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STANDARD POROCOAT MODIFIED MEDIAL ASPECT AML HIP is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1987-05-01 under 510(k) number K870699. 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 STANDARD POROCOAT MODIFIED MEDIAL ASPECT AML HIP?

STANDARD POROCOAT MODIFIED MEDIAL ASPECT AML HIP is a medical device that received FDA 510(k) clearance on 1987-05-01. The listed applicant is Depuy, Inc.. The 510(k) number is K870699.

When did STANDARD POROCOAT MODIFIED MEDIAL ASPECT AML HIP receive FDA 510(k) clearance?

STANDARD POROCOAT MODIFIED MEDIAL ASPECT AML HIP received FDA 510(k) clearance on 1987-05-01, under 510(k) number K870699.

Who is the listed applicant for STANDARD POROCOAT MODIFIED MEDIAL ASPECT AML HIP?

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 STANDARD POROCOAT MODIFIED MEDIAL ASPECT AML HIP?

The FDA product code for STANDARD POROCOAT MODIFIED MEDIAL ASPECT AML HIP is JDI.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: JDI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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