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DEPUY 1 BONE CEMENT

FDA premarket approval P960001 · decided 1997-02-11

Approval details

PMA number
P960001
Trade name
DEPUY 1 BONE CEMENT
Generic name
BONE CEMENT
Applicant
Depuy, Inc.
Date received
1996-01-11
Decision date
1997-02-11
Days to decision
397 days
Decision code
APRL
Product code
LOD
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
APPROVAL FOR THE DEPUY 1 BONE CEMENT. THIS DEVICE IS INDICATED FOR THE FIXATION OF PROSTHESES TO LIVING BONE IN ORTHOPEDIC MUSCULOSKELETAL SURGICAL PROCEDURES FOR THEUMATOID ARTHRITIS, OSTEOARTHRITIS, TRAUMATIC ARTHRITIS, OSTEOPOROSIS, AVASCULAR NECROSIS, COLLAGEN DISEASE, SEVERE JOINT DESTRUCTION SECONDARY TO TRAUMA OR OTHER CONDITIONS AND REVISION OF PREVIOUS ARTHOROPLASTY.

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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