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FDA 510(k)

LOCON-T DISTAL RADIAL PLATE

K-Number: K994061 · 2000-02-14

ApplicantWrightmedicaltechnologyinc
Decision Date2000-02-14
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LOCON-T DISTAL RADIAL PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2000-02-14 under 510(k) number K994061. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOCON-T DISTAL RADIAL PLATE?

LOCON-T DISTAL RADIAL PLATE is a medical device that received FDA 510(k) clearance on 2000-02-14. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K994061.

When did LOCON-T DISTAL RADIAL PLATE receive FDA 510(k) clearance?

LOCON-T DISTAL RADIAL PLATE received FDA 510(k) clearance on 2000-02-14, under 510(k) number K994061.

Who is the listed applicant for LOCON-T DISTAL RADIAL PLATE?

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

What is the FDA product code for LOCON-T DISTAL RADIAL PLATE?

The FDA product code for LOCON-T DISTAL RADIAL PLATE is HRS.

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Related Devices (Code: HRS)

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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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