Atlas FDA

LCS TOTAL KNEE SYSTEM

FDA premarket approval P830055/S082 · decided 2002-10-04

Approval details

PMA number
P830055
Supplement
S082
Supplement type
Normal 180 Day Track
Supplement reason
Express GMP Supplement
Trade name
LCS TOTAL KNEE SYSTEM
Generic name
Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing
Applicant
Depuy, Inc.
Date received
2002-03-28
Decision date
2002-10-04
Days to decision
190 days
Decision code
APPR
Product code
NJL
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
APPROVAL FOR AN ADDITIONAL STERILIZATION FACILITY LOCATED AT ISOTRON, BERKSHIRE, ENGLAND.

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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