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INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE

FDA premarket approval P000058/S002 · decided 2004-07-29

Approval details

PMA number
P000058
Supplement
S002
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
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
2002-10-24
Decision date
2004-07-29
Days to decision
644 days
Decision code
APPR
Product code
NEK
Advisory committee
Orthopedic
Expedited review
No
Location
Memphis, TN
Statement
APPROVAL FOR 1) THE EXTENSION OF THE LEVELS OF USE OF THE DEVICE FROM L4-S1 TO L2-S1 2) MODIFICATION OF THE INDICATION TO ALLOW FOR THE DEVICE TO BE USED IN SUBJECTS WHO MAY HAVE RETROLISTHESIS IN CONJUNCTION WITH DEGENERATIVE DISC DISEASE 3) CHANGE IN STORAGE TEMPERATURE LIMIT AND 4) REVISIONS TO INSTRUCTION FOR USE.

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