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FDA 510(k)

MULLER-TYPE FEMORAL COMPONENT

K-Number: K903243 · 1990-07-30

ApplicantOnyx Medical Corp.
Decision Date1990-07-30
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MULLER-TYPE FEMORAL COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Onyx Medical Corp.. It received FDA 510(k) clearance on 1990-07-30 under 510(k) number K903243. 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 MULLER-TYPE FEMORAL COMPONENT?

MULLER-TYPE FEMORAL COMPONENT is a medical device that received FDA 510(k) clearance on 1990-07-30. The listed applicant is Onyx Medical Corp.. The 510(k) number is K903243.

When did MULLER-TYPE FEMORAL COMPONENT receive FDA 510(k) clearance?

MULLER-TYPE FEMORAL COMPONENT received FDA 510(k) clearance on 1990-07-30, under 510(k) number K903243.

Who is the listed applicant for MULLER-TYPE FEMORAL COMPONENT?

The FDA 510(k) record lists Onyx Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULLER-TYPE FEMORAL COMPONENT?

The FDA product code for MULLER-TYPE FEMORAL COMPONENT is JDI.

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Other records listing Onyx Medical Corp. as applicant

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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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