Orthopaedic Biosystems, Ltd. is one of 9563 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthopaedic Biosystems, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: POLYMER OBL SB ANCHOR / SUTURE COMBINATION, POLYMER THREADED ANCHOR, POLYMER THREADED ANCHOR / SUTURE COMBINATION
11
Total
9
Cleared
0
Denied
Orthopaedic Biosystems, Ltd. has 9 FDA 510(k) cleared orthopedic devices. Based in Scotsdale, US.
Historical record: 9 cleared submissions from 1995 to 2000.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Orthopaedic Biosystems, Ltd.
11 devices
Cleared
Apr 03, 2000
OBL 2.0 MM MINI TAC ANCHOR, MODEL 10-1629-01
Orthopedic
21d
Cleared
Mar 04, 1999
POLYMER OBL SB ANCHOR / SUTURE COMBINATION
Orthopedic
189d
Cleared
Dec 16, 1998
POLYMER THREADED ANCHOR
Orthopedic
97d
Cleared
Nov 20, 1998
POLYMER THREADED ANCHOR / SUTURE COMBINATION
Orthopedic
88d
Cleared
Feb 06, 1998
PEBA ANCHOR/SUTURE COMBINATION
Orthopedic
228d
Cleared
Nov 15, 1996
CANCELLOUS SCREW WASHER
Orthopedic
77d
Cleared
Nov 13, 1996
GUIDE WIRES FOR CANNULATED SCREWS
Orthopedic
75d
Cleared
Nov 06, 1996
THREADED FIXATION PIN
Orthopedic
68d
Cleared
Aug 23, 1996
COMPRESSION SCREW
Orthopedic
37d
Cleared
Oct 31, 1995
PEBA ANCHOR (MULTIPLE SIZES)
Orthopedic
216d
Cleared
Aug 25, 1995
SB ANCHOR
Orthopedic
431d