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FDA 510(k)

ULTIMA SIZE 0 CEMENTED FEMORAL STEM

K-Number: K953200 · 1996-01-31

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1996-01-31
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

ULTIMA SIZE 0 CEMENTED FEMORAL STEM 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 1996-01-31 under 510(k) number K953200. 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 ULTIMA SIZE 0 CEMENTED FEMORAL STEM?

ULTIMA SIZE 0 CEMENTED FEMORAL STEM is a medical device that received FDA 510(k) clearance on 1996-01-31. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K953200.

When did ULTIMA SIZE 0 CEMENTED FEMORAL STEM receive FDA 510(k) clearance?

ULTIMA SIZE 0 CEMENTED FEMORAL STEM received FDA 510(k) clearance on 1996-01-31, under 510(k) number K953200.

Who is the listed applicant for ULTIMA SIZE 0 CEMENTED FEMORAL STEM?

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 SIZE 0 CEMENTED FEMORAL STEM?

The FDA product code for ULTIMA SIZE 0 CEMENTED FEMORAL STEM is JDI.

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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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