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FDA 510(k)

ULTIMA ACETABULAR ROOF REINFORCEMENT RING

K-Number: K980286 · 1998-04-03

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1998-04-03
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ULTIMA ACETABULAR ROOF REINFORCEMENT RING 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 1998-04-03 under 510(k) number K980286. 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 ULTIMA ACETABULAR ROOF REINFORCEMENT RING?

ULTIMA ACETABULAR ROOF REINFORCEMENT RING is a medical device that received FDA 510(k) clearance on 1998-04-03. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K980286.

When did ULTIMA ACETABULAR ROOF REINFORCEMENT RING receive FDA 510(k) clearance?

ULTIMA ACETABULAR ROOF REINFORCEMENT RING received FDA 510(k) clearance on 1998-04-03, under 510(k) number K980286.

Who is the listed applicant for ULTIMA ACETABULAR ROOF REINFORCEMENT RING?

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 ULTIMA ACETABULAR ROOF REINFORCEMENT RING?

The FDA product code for ULTIMA ACETABULAR ROOF REINFORCEMENT RING 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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