FDA 510(k) Applications Submitted by ERIC BANNON

FDA 510(k) Number Submission Date Device Name Applicant
K970089 01/10/1997 INNOVASIVE 2.8MM AND 3.5MM ROC LF SUTURE BONE FASTENER INNOVASIVE DEVICES, INC.
K970316 01/24/1997 INNOVASIVE 8MM LIGAMENT FASTENER INNOVASIVE DEVICES, INC.
K970423 02/04/1997 INNOVASIVE ROCLET BONE TUNNEL AUGMENTATION DEVICE INNOVASIVE DEVICES, INC.
K980681 02/20/1998 INNOVASIVE DEVICES MENISCAL SCREW INNOVASIVE DEVICES, INC.
K060522 02/27/2006 SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM SCANDIUS BIOMEDICAL, INC.
K000694 03/01/2000 PECTOFIX DYNAMIC STERNAL FIXATION SYSTEM (DSF) PECTOFIX, INC.
K981340 04/13/1998 INNOVASIVE DEVICES MENISCAL DART REPAIR SYSTEM INNOVASIVE DEVICES, INC.
K031262 04/21/2003 ENDOSCOPIC PLICATION SYSTEM, MODEL 160-00760 NDO SURGICAL, INC.
K982266 06/29/1998 HYDROCISION ARTHROJET SYSTEM HYDROCISION, INC.
K041749 06/29/2004 SCANDIUS ACL RECONSTRUCTION SYSTEM SCANDIUS BIOMEDICAL, INC.
K041961 07/21/2004 SCANDIUS ABSORBABLE ACL RECONSTRUCTION SYSTEM SCANDIUS BIOMEDICAL, INC.
K963402 08/29/1996 INNOVASIVE 2.8MM ROC SUTURE BONE FASTENER AND 3.5MM ROC SUTURE BONE FASTENER INNOVASIVE DEVICES, INC.
K973313 09/03/1997 INNOVASIVE DEVICES Y-KNOT SUTURE CLIP INNOVASIVE DEVICES, INC.
K973323 09/04/1997 ACL CLIP-IN INNOVASIVE DEVICES, INC.
K032820 09/10/2003 MODIFICATION TO ENDOSCOPIC PLICATION SYSTEM NDO SURGICAL, INC.
K954338 09/18/1995 INNOVASIVE 1.9MM ROC SUTURE BONE FASTENER INNOVASIVE DEVICES, INC.
K023234 09/27/2002 ENDOSCOPIC PLICATION SYSTEM NDO SURGICAL, INC.
K052810 10/04/2005 SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM SCANDIUS BIOMEDICAL, INC.
K973874 10/10/1997 ACL CLIP-IN PLATE INNOVASIVE DEVICES, INC.
K983560 10/13/1998 INNOVASIVE DEVICES INTRATUNNEL TIBIAL FIXATION FASTENER INNOVASIVE DEVICES, INC.
K964945 12/10/1996 INNOVASIVE DEVICES ROTATOR CUFF FASTNER INNOVASIVE DEVICES, INC.
K003951 12/21/2000 PECTOFIX STERNAL REPAIR WIRE PECTOFIX, INC.


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