Biologically Oriented Prostheses is one of 25895 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biologically Oriented Prostheses - FDA 510(k) Cleared Devices
Recent clearances: WUJIN #3 TIBIAL NAIL, BIOPRO RIMMED ACETABULAR COMPOMENT, RIOPRO COBALT TRAPEZIOMETARCARPAL RESURFACING COMPONENT
9
Total
7
Cleared
0
Denied
Biologically Oriented Prostheses has 7 FDA 510(k) cleared medical devices. Based in Port Huron, US.
Historical record: 7 cleared submissions from 1995 to 2000. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Biologically Oriented Prostheses Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biologically Oriented Prostheses
9 devices
Cleared
Oct 30, 2000
WUJIN #3 TIBIAL NAIL
Orthopedic
90d
Cleared
Sep 22, 1999
BIOPRO RIMMED ACETABULAR COMPOMENT
Orthopedic
90d
Cleared
Feb 03, 1997
RIOPRO COBALT TRAPEZIOMETARCARPAL RESURFACING COMPONENT
Orthopedic
88d
Cleared
Oct 03, 1996
HORIZON HIP SYSTEM
Orthopedic
79d
Cleared
Aug 08, 1996
TOWNLEY TOTAL ELBOW SYSTEM
Orthopedic
223d
Cleared
Jan 18, 1996
BIOPRO HEMI-ENDO MODULAR CERAMIC HEAD
Orthopedic
93d
Cleared
Dec 28, 1995
TOWNLEY ALL POLY ACETABULAR CUP
Orthopedic
196d
Cleared
Sep 27, 1995
BIOPRO HEMI-ENDO MODULAR CERAMIC HEAD
Orthopedic
89d
Cleared
Jun 19, 1995
VARIOUS UHMWP HIP & KNEE JOINT PROSTHESIS MODIFIED
Orthopedic
87d