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FDA 510(k) Application Details - K060180
Device Classification Name
Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
More FDA Info for this Device
510(K) Number
K060180
Device Name
Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
Applicant
REGENERATION TECHNOLOGIES, INC.
11621 RESEARCH CIR.
P.O. BOX 2650
ALACHUA, FL 32616-2650 US
Other 510(k) Applications for this Company
Contact
Lisa Simpson
Other 510(k) Applications for this Contact
Regulation Number
888.3045
More FDA Info for this Regulation Number
Classification Product Code
MBP
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/23/2006
Decision Date
09/06/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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