LODA WRIST PROSTHESIS— 510(k) K790774

Substantially Equivalent

Depuy, Inc.

FDA 510(k) clearance K790774 for LODA WRIST PROSTHESIS, Substantially Equivalent on 1979-08-03. Applicant: Depuy, Inc.. Device class: 2.

Clearance details

Applicant: Depuy, Inc.
Product code: Code KWM
Device class: Class 2
Regulation: 21 CFR 888.3800
Advisory panel: Orthopedic
Date received: 1979-04-20
Decision date: 1979-08-03
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
K803031 — LAURE WRIST IMPLANT1982-06-29
K800602 — TALEISNIK TOTAL WRIST PROSTHESIS1980-08-27
K801157 — WEBER-MAYO WRIST1980-08-04

More clearances from Depuy, Inc.

K043058 — PINNACLE CONSTRAINED ACETABULAR LINERS2005-03-14
K042664 — LPS UPPER EXTREMITY2004-12-08
K041085 — LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARY2004-07-22
K033959 — LPS2004-07-01
K040544 — DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -0622004-05-28

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