Aesculap Implant System, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aesculap Implant System, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Aesculap Implant System, Inc. has 18 FDA 510(k) cleared orthopedic devices. Based in Center Valley, US.
Historical record: 18 cleared submissions from 2007 to 2014.
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 - Aesculap Implant System, Inc.
18 devices
Cleared
Dec 19, 2014
AIS Odontoid Fracture Fixation System
Orthopedic
88d
Cleared
Oct 29, 2014
AIS MODULIFT VBR SYSTEM
Orthopedic
85d
Cleared
Apr 17, 2014
AIS MODULIFT VBR SYSTEM
Orthopedic
125d
Cleared
Oct 30, 2013
PLASMAFIT ACETABULAR CUP AND VITELENE INSERT
Orthopedic
414d
Cleared
Aug 13, 2013
S4C NAVIGATION INSTRUMENTS
Orthopedic
137d
Cleared
Apr 15, 2013
AESCULAP CESPACE XP
Orthopedic
117d
Cleared
Apr 11, 2013
S4 SPINAL SYSTEM
Orthopedic
64d
Cleared
Oct 26, 2012
COLUMBUS REVISION KNEE SYSTEM
Orthopedic
30d
Cleared
Nov 21, 2011
S4 SPINAL SYSTEM
Orthopedic
81d
Cleared
Jul 30, 2010
VEGA KNEE SYSTEM
Orthopedic
85d
Cleared
Jul 23, 2010
S4 CERVICAL OCCIPITAL PLATE SPINAL SYSTEM
Orthopedic
185d
Cleared
Mar 04, 2010
AESCULAP HYDROLIFT VBR SYSTEM
Orthopedic
491d