Orthopaedic Innovations, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthopaedic Innovations, Inc. - FDA 510(k) Cleared Devices
8
Total
7
Cleared
0
Denied
Orthopaedic Innovations, Inc. has 7 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 7 cleared submissions from 1995 to 2002. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthopaedic Innovations, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Orthopaedic Innovations, Inc.
8 devices
Cleared
Apr 15, 2002
ORTHOPAEDIC INNOVATIONS RENEWAL ACETABULAR CUP SYSTEM
Orthopedic
89d
Cleared
Dec 04, 1998
COBRA EXTERNAL FIXATOR
Orthopedic
32d
Cleared
Sep 23, 1996
PRIME MODULAR ENDO HEAD
Orthopedic
77d
Cleared
Mar 18, 1996
PRACTIFIX EXTERNAL FIXATION SYSTEM
Orthopedic
76d
Cleared
Feb 20, 1996
PRIME CEMENTED CALCAR FEMORAL STEMS
Orthopedic
71d
Cleared
Jan 26, 1996
PRIME FEMORAL CEMENT PLUG
Orthopedic
37d
Cleared
Sep 13, 1995
PRIME CEMENTED SMALL FEMORAL STEM
Orthopedic
75d
Cleared
Apr 07, 1995
PRIME CEMENTED HIP SYSTEM
Orthopedic
438d