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FDA 510(k)

SCORPIO INSET PATELLAR COMPONENT

K-Number: K020830 · 2002-06-06

ApplicantHowmedica Osteonics Corp.
Decision Date2002-06-06
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SCORPIO INSET PATELLAR COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 2002-06-06 under 510(k) number K020830. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCORPIO INSET PATELLAR COMPONENT?

SCORPIO INSET PATELLAR COMPONENT is a medical device that received FDA 510(k) clearance on 2002-06-06. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K020830.

When did SCORPIO INSET PATELLAR COMPONENT receive FDA 510(k) clearance?

SCORPIO INSET PATELLAR COMPONENT received FDA 510(k) clearance on 2002-06-06, under 510(k) number K020830.

Who is the listed applicant for SCORPIO INSET PATELLAR COMPONENT?

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

What is the FDA product code for SCORPIO INSET PATELLAR COMPONENT?

The FDA product code for SCORPIO INSET PATELLAR COMPONENT is JWH.

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Related Devices (Code: JWH)

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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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