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FDA 510(k)

THREADED ACETABULAR COMPONENT

K-Number: K870445 · 1987-03-20

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1987-03-20
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THREADED ACETABULAR COMPONENT 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 1987-03-20 under 510(k) number K870445. 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 THREADED ACETABULAR COMPONENT?

THREADED ACETABULAR COMPONENT is a medical device that received FDA 510(k) clearance on 1987-03-20. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K870445.

When did THREADED ACETABULAR COMPONENT receive FDA 510(k) clearance?

THREADED ACETABULAR COMPONENT received FDA 510(k) clearance on 1987-03-20, under 510(k) number K870445.

Who is the listed applicant for THREADED ACETABULAR COMPONENT?

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 THREADED ACETABULAR COMPONENT?

The FDA product code for THREADED ACETABULAR COMPONENT 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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