COLLAGRAFT(TM) BONE GRAFT MATRIX

FDA Premarket Approval P900039 S006

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

DeviceCOLLAGRAFT(TM) BONE GRAFT MATRIX
Generic NameFiller, Bone Void, Non-osteoinduction
ApplicantNEUCOLL, INC.
Date Received1994-11-01
Decision Date1995-03-21
PMAP900039
SupplementS006
Product CodeMBS 
Advisory CommitteeOrthopedic
Supplement TypeNormal 180 Day Track
Supplement ReasonLocation Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product No
Applicant Address NEUCOLL, INC. 105 Cooper Ct. los Gatos, CA 95032-7604

Supplemental Filings

Supplement NumberDateSupplement Type
P900039Original Filing
S015 2004-12-27 30-day Notice
S014
S013 2004-04-30 Normal 180 Day Track No User Fee
S012 2002-09-12 30-day Notice
S011 2001-09-19 Normal 180 Day Track
S010 1998-11-23 Real-time Process
S009 1995-10-10 Normal 180 Day Track
S008 1995-07-28 Normal 180 Day Track
S007 1995-01-24 Special (immediate Track)
S006 1994-11-01 Normal 180 Day Track
S005 1994-09-20 Special (immediate Track)
S004
S003 1993-10-01 Normal 180 Day Track
S002 1993-07-02 Normal 180 Day Track
S001 1992-12-03 Normal 180 Day Track

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