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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