Aesculap Implant Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aesculap Implant Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ArcadiusXP C Spinal System, AESCULAP PEEK XP SPINAL IMPLANT SYSTEM, S4 SPINAL SYSTEM
22
Total
22
Cleared
0
Denied
Aesculap Implant Systems, Inc. has 22 FDA 510(k) cleared orthopedic devices. Based in Center Valley, US.
Historical record: 22 cleared submissions from 2007 to 2016.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Aesculap AG as regulatory consultant.
FDA 510(k) Regulatory Record - Aesculap Implant Systems, Inc.
22 devices
Cleared
May 25, 2016
ArcadiusXP C Spinal System
Orthopedic
159d
Cleared
Jan 22, 2014
AESCULAP PEEK XP SPINAL IMPLANT SYSTEM
Orthopedic
170d
Cleared
Mar 12, 2013
S4 SPINAL SYSTEM
Orthopedic
82d
Cleared
Dec 12, 2012
S4 SPINAL SYSTEM
Orthopedic
42d
Cleared
Aug 04, 2011
AESCULAP SIBD XP SPINAL SYSTEM
Orthopedic
105d
Cleared
Dec 02, 2010
LAMINOPLASY PLATING SYSTEM
Orthopedic
27d
Cleared
Jul 20, 2010
AESCULAP IMPLANT SYSTEMS SIBD SPINAL SYSTEM
Orthopedic
120d
Cleared
Sep 22, 2009
EXCIA TOTAL HIP SYSTEM M AN ML FEMORAL STEM
Orthopedic
69d
Cleared
Jul 02, 2009
MILI (MINIMALLY INVASIVE LUMBAR IMPLANT) SYSTEM
Orthopedic
267d
Cleared
Mar 04, 2009
AESCULAP CESPACE PEEK INTERVERTEBRAL BODY FUSION SYSTEM
Orthopedic
114d
Cleared
Jan 15, 2009
MODIFICATION TO: METHA HIP SYSTEM
Orthopedic
51d
Cleared
Nov 20, 2008
BIOLOX DELTA CERAMIC FEMORAL HEAD
Orthopedic
44d