LAURE WRIST IMPLANT— 510(k) K803031

Substantially Equivalent

Laure Prosthetics, Inc.

FDA 510(k) clearance K803031 for LAURE WRIST IMPLANT, Substantially Equivalent on 1982-06-29. Applicant: Laure Prosthetics, Inc.. Device class: 2.

Clearance details

Applicant: Laure Prosthetics, Inc.
Product code: Code KWM
Device class: Class 2
Regulation: 21 CFR 888.3800
Advisory panel: Orthopedic
Date received: 1980-11-28
Decision date: 1982-06-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KWM

K880156 — VOLZ TOTAL WRIST PROSTHESIS1988-02-17
K872502 — M.W.P. WRIST PROSTHESIS1987-07-23
K800602 — TALEISNIK TOTAL WRIST PROSTHESIS1980-08-27
K801157 — WEBER-MAYO WRIST1980-08-04
K790774 — LODA WRIST PROSTHESIS1979-08-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.