Atlas FDA

INFUSE BONE GRAFT

FDA premarket approval P000054/S020 · decided 2009-02-20

Approval details

PMA number
P000054
Supplement
S020
Supplement type
Real-Time Process
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
INFUSE BONE GRAFT
Generic name
Filler, recombinant human bone morphogenetic protein, collagen scaffold, osteoinduction
Applicant
Medtronic Sofamor Danek USA, Inc.
Date received
2008-12-23
Decision date
2009-02-20
Days to decision
59 days
Decision code
APPR
Product code
MPW
Advisory committee
Orthopedic
Expedited review
No
Location
Memphis, TN
Statement
APPROVAL FOR CHANGES IN THE EXTERIOR CARTONS USED TO SHIP ONE OR MORE UNITS OF INFUSE BONE GRAFT.

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