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INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE

FDA premarket approval P000058/S009 · decided 2005-04-20

Approval details

PMA number
P000058
Supplement
S009
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE
Generic name
Filler, recombinant human bone morphogenetic protein, collagen scaffold with metal prosthesis, osteoinduction
Applicant
Medtronic Sofamor Danek USA, Inc.
Date received
2004-04-20
Decision date
2005-04-20
Days to decision
365 days
Decision code
APPR
Product code
NEK
Advisory committee
Orthopedic
Expedited review
No
Location
Memphis, TN
Statement
APPROVAL FOR TWO CHANGES TO THE PROCESSING OF THE RHBMP-2 COMPONENT OF THE DEVICE - THE USE OF A NEW WORKING CELL BANK AND THE USE OF A LONGER HOLD-TIME (<=120 HOURS AT 2-8 DEGREES C COMPARED TO THE CURRENT 24 HOURS) FOR THE MATREX CELLUFINE SULFATE COLUMN.

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