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FDA 510(k)

TALEISNIK TOTAL WRIST PROSTHESIS

K-Number: K800602 · 1980-08-27

ApplicantDow Corning Wright
Decision Date1980-08-27
Product CodeKWM
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TALEISNIK TOTAL WRIST PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Wright. It received FDA 510(k) clearance on 1980-08-27 under 510(k) number K800602. The device is classified under product code KWM. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TALEISNIK TOTAL WRIST PROSTHESIS?

TALEISNIK TOTAL WRIST PROSTHESIS is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Dow Corning Wright. The 510(k) number is K800602.

When did TALEISNIK TOTAL WRIST PROSTHESIS receive FDA 510(k) clearance?

TALEISNIK TOTAL WRIST PROSTHESIS received FDA 510(k) clearance on 1980-08-27, under 510(k) number K800602.

Who is the listed applicant for TALEISNIK TOTAL WRIST PROSTHESIS?

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

What is the FDA product code for TALEISNIK TOTAL WRIST PROSTHESIS?

The FDA product code for TALEISNIK TOTAL WRIST PROSTHESIS is KWM.

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Related Devices (Code: KWM)

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K880156VOLZ TOTAL WRIST PROSTHESISBiomet, Inc.K872502M.W.P. WRIST PROSTHESISProtek, Inc.K803031LAURE WRIST IMPLANTLaure Prosthetics, Inc.K801157WEBER-MAYO WRISTDepuy, Inc.K790774LODA WRIST PROSTHESISDepuy, Inc.

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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