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FDA 510(k)

ULTIMA FX FEMORAL HIP STEMS

K-Number: K963885 · 1996-12-09

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1996-12-09
Product CodeKWY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ULTIMA FX FEMORAL HIP STEMS 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 1996-12-09 under 510(k) number K963885. The device is classified under product code KWY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTIMA FX FEMORAL HIP STEMS?

ULTIMA FX FEMORAL HIP STEMS is a medical device that received FDA 510(k) clearance on 1996-12-09. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K963885.

When did ULTIMA FX FEMORAL HIP STEMS receive FDA 510(k) clearance?

ULTIMA FX FEMORAL HIP STEMS received FDA 510(k) clearance on 1996-12-09, under 510(k) number K963885.

Who is the listed applicant for ULTIMA FX FEMORAL HIP STEMS?

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 FX FEMORAL HIP STEMS?

The FDA product code for ULTIMA FX FEMORAL HIP STEMS is KWY.

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Related Devices (Code: KWY)

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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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