Atlas FDA

LCS Total Knee System

FDA premarket approval P830055/S198 · decided 2018-06-27

Approval details

PMA number
P830055
Supplement
S198
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
LCS Total Knee System
Generic name
Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing
Applicant
Depuy, Inc.
Date received
2018-03-29
Decision date
2018-06-27
Days to decision
90 days
Decision code
APPR
Product code
NJL
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
Approval for adding the ATTUNE Cemented Tibial Bases, Rotating Platform (RP) as an extension to the ATTUNE Knee System, and to expand compatibility of the ATTUNE Cementless PS Femoral device to both the ATTUNE Cemented Tibial Base, RP and the ATTUNE Cementless RP Tibial Base.

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510(k) clearances by this applicant

RecordFirmDate
PINNACLE CONSTRAINED ACETABULAR LINERS (K043058)Depuy, Inc.2005-03-14
LPS UPPER EXTREMITY (K042664)Depuy, Inc.2004-12-08
LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARY (K041085)Depuy, Inc.2004-07-22
LPS (K033959)Depuy, Inc.2004-07-01
DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062 (K040544)Depuy, Inc.2004-05-28
DELTA SHOULDER (K021478)Depuy, Inc.2003-11-18
DEPUY ACE UNIVERSAL AND TROCH ENTRY FEMORAL NAIL SYSTEMS (K033329)Depuy, Inc.2003-11-14
DEPUY SIGMA TIBIAL INSERTS AND CO-CR TIBIAL TRAYS (K032151)Depuy, Inc.2003-09-26