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INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPARED FUSION DEVICE

FDA premarket approval P000058/S015 · decided 2005-02-04

Approval details

PMA number
P000058
Supplement
S015
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPARED FUSION DEVICE
Generic name
Filler, recombinant human bone morphogenetic protein, collagen scaffold with metal prosthesis, osteoinduction
Applicant
Medtronic Sofamor Danek USA, Inc.
Date received
2004-11-15
Decision date
2005-02-04
Days to decision
81 days
Decision code
APPR
Product code
NEK
Advisory committee
Orthopedic
Expedited review
No
Location
Memphis, TN
Statement
APPROVAL FOR THE INCLUSION OF ADDITIONAL FUSION CAGE COMPONENT DESIGNS. SPECIFICALLY, THESE DESIGN CHANGES INVOLVED THE INCORPORATION OF A ROUNDED PROFILE TO THE CLOSED END OF THE TAPERED CAGE COMPONENTS. THE MODIFIED TAPERED CAGE COMPONENTS CAN ONLY BE IMPLANTED VIA AN ANTERIOR OPEN SURGICAL APPROACH.

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