Centerpulse Orthopedics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Centerpulse Orthopedics, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Centerpulse Orthopedics, Inc. has 10 FDA 510(k) cleared orthopedic devices. Based in Austin, US.
Historical record: 10 cleared submissions from 2003 to 2004.
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 - Centerpulse Orthopedics, Inc.
10 devices
Cleared
Oct 18, 2004
ALPHA METASUL 28MM AND 32MM ACETABULAR INSERTS, STANDARD AND HOODED
Orthopedic
304d
Cleared
Sep 15, 2004
EPSILON METASUL 32MM ACETABULAR INSERTS, STANDARD AND HOODED
Orthopedic
301d
Cleared
Aug 27, 2004
DURASUL BIPOLAR
Orthopedic
137d
Cleared
Mar 05, 2004
NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM
Orthopedic
88d
Cleared
Dec 17, 2003
MODIFICATION TO ALLOCLASSIC ZWEYMULLER SL OFFSET FEMORAL STEM
Orthopedic
26d
Cleared
Oct 24, 2003
CONVERGE RETI-LOCK MULTI-HOLE REINFORCEMENT CUP
Orthopedic
86d
Cleared
Oct 03, 2003
EPSILON DURASUL CONSTRAINED ACETABULAR LINER
Orthopedic
193d
Cleared
Sep 22, 2003
WAGNER CONE PROSTHESIS
Orthopedic
52d
Cleared
Jul 14, 2003
TIBIAL SPACER FOR THE NATURAL-KNEE II CEMENTED MODULAR TIBIAL BASEPLATE
Orthopedic
90d
Cleared
Mar 06, 2003
ALLOCLASSIC ZWEYMUELLER SL/SLL FEMORAL STEM
Orthopedic
30d