Atlas FDA

DEPUY 3 BONE CEMENT

FDA premarket approval P960001/S006 · decided 1999-09-20

Approval details

PMA number
P960001
Supplement
S006
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
DEPUY 3 BONE CEMENT
Generic name
BONE CEMENT
Applicant
Depuy, Inc.
Date received
1998-07-06
Decision date
1999-09-20
Days to decision
441 days
Decision code
APPR
Product code
LOD
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
Approval for a change in the bone cement formulation to alter the handling characteristics.

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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