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FDA 510(k)

POROUS COATED ACETABULAR CUP

K-Number: K873585 · 1987-10-28

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1987-10-28
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

POROUS COATED ACETABULAR CUP is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1987-10-28 under 510(k) number K873585. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the POROUS COATED ACETABULAR CUP?

POROUS COATED ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 1987-10-28. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K873585.

When did POROUS COATED ACETABULAR CUP receive FDA 510(k) clearance?

POROUS COATED ACETABULAR CUP received FDA 510(k) clearance on 1987-10-28, under 510(k) number K873585.

Who is the listed applicant for POROUS COATED ACETABULAR CUP?

The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POROUS COATED ACETABULAR CUP?

The FDA product code for POROUS COATED ACETABULAR CUP 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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