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FDA 510(k)

NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS

K-Number: K800494 · 1980-03-18

ApplicantDepuy, Inc.
Decision Date1980-03-18
Product CodeHSD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1980-03-18 under 510(k) number K800494. The device is classified under product code HSD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS?

NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS is a medical device that received FDA 510(k) clearance on 1980-03-18. The listed applicant is Depuy, Inc.. The 510(k) number is K800494.

When did NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS receive FDA 510(k) clearance?

NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS received FDA 510(k) clearance on 1980-03-18, under 510(k) number K800494.

Who is the listed applicant for NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS?

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

What is the FDA product code for NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS?

The FDA product code for NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS is HSD.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: HSD)

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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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