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UNICOMPARTMENTAL DEVICE CONFIGURATION OF THE LCS TOTAL KNEE SYSTEM

FDA premarket approval P910016/S014 · decided 2005-09-26

Approval details

PMA number
P910016
Supplement
S014
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
UNICOMPARTMENTAL DEVICE CONFIGURATION OF THE LCS TOTAL KNEE SYSTEM
Generic name
PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, UNCONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER
Applicant
Depuy, Inc.
Date received
2005-05-23
Decision date
2005-09-26
Days to decision
126 days
Decision code
APPR
Product code
MBD
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
APPROVAL FOR CHANGES TO THE POST-APPROVAL STUDY.

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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