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LSC TOTAL KNEE SYSTEM

FDA premarket approval P830055/S129 · decided 2013-11-29

Approval details

PMA number
P830055
Supplement
S129
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
LSC TOTAL KNEE SYSTEM
Generic name
Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing
Applicant
Depuy, Inc.
Date received
2012-11-13
Decision date
2013-11-29
Days to decision
381 days
Decision code
APPR
Product code
NJL
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
APPROVAL FOR MANUFACTURING SITES LOCATED AT STERIS ISOMEDIX, CHESTER, NEW YORK, AND SYNERGY HEALTH SWITZERLAND, DÄNIKEN, SWITZERLAND. BOTH FACILITIES WILL PERFORM STERILIZATION OPERATIONS FOR THE LCS TOTAL KNEE SYSTEM.

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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