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FDA 510(k)

DORR HIP PROSTHESIS FEMORAL COMPONENT

K-Number: K842360 · 1984-10-02

ApplicantCarbomedics, Inc.
Decision Date1984-10-02
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DORR HIP PROSTHESIS FEMORAL COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Carbomedics, Inc.. It received FDA 510(k) clearance on 1984-10-02 under 510(k) number K842360. 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 DORR HIP PROSTHESIS FEMORAL COMPONENT?

DORR HIP PROSTHESIS FEMORAL COMPONENT is a medical device that received FDA 510(k) clearance on 1984-10-02. The listed applicant is Carbomedics, Inc.. The 510(k) number is K842360.

When did DORR HIP PROSTHESIS FEMORAL COMPONENT receive FDA 510(k) clearance?

DORR HIP PROSTHESIS FEMORAL COMPONENT received FDA 510(k) clearance on 1984-10-02, under 510(k) number K842360.

Who is the listed applicant for DORR HIP PROSTHESIS FEMORAL COMPONENT?

The FDA 510(k) record lists Carbomedics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DORR HIP PROSTHESIS FEMORAL COMPONENT?

The FDA product code for DORR HIP PROSTHESIS FEMORAL 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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