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DURALOC OPTION CERAMIC ON CERAMIC HIP SYSTEM

FDA premarket approval P040023/S002 · decided 2005-12-12

Approval details

PMA number
P040023
Supplement
S002
Supplement type
Special (Immediate Track)
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
DURALOC OPTION CERAMIC ON CERAMIC HIP SYSTEM
Generic name
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
Applicant
DePuy Orthopaedics, Inc.
Date received
2005-11-10
Decision date
2005-12-12
Days to decision
32 days
Decision code
APPR
Product code
MRA
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
APPROVAL FOR CHANGES IN QUALITY CONTROLS TO VARIOUS COMPONENTS OF THIS SYSTEM. THESE CHANGES INCLUDE MODIFICATION TO SEVERAL MANUFACTURING PROCESS SPECIFICATIONS (MPS) FOR GAMMA VACUUM FOIL (GVF) PACKAGED PRODUCTS: 1) TO ADD PHYSICAL SEPARATION BARRIERS TO THE SEALING MACHINE TO PREVENT ADJACENT FOIL POUCHES FROM OVERLAPPING DURING THE SEALING OPERATION, AND 2) TO REQUIRE A SECOND 100% INSPECTION OF THE SEAL INTEGRITY OF EACH PACKAGE PRIOR TO SHIPMENT.

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510(k) clearances by this applicant

RecordFirmDate
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CUPTIMIZE™ Advanced (K231503)DePuy Orthopaedics, Inc.2023-08-22
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