Medical Device Manufacturer · US , Center Valley , PA

Aesculap Implant Systems, Inc. - FDA 510(k) Cleared Devices

22 submissions · 22 cleared · Since 2007
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.

FDA 510(k) Regulatory Record - Aesculap Implant Systems, Inc.
22 devices
1-12 of 22
Cleared May 25, 2016
ArcadiusXP C Spinal System
K153629 · OVE
Orthopedic · 159d
Cleared Jan 22, 2014
AESCULAP PEEK XP SPINAL IMPLANT SYSTEM
K132421 · MAX
Orthopedic · 170d
Cleared Mar 12, 2013
S4 SPINAL SYSTEM
K123939 · NKB
Orthopedic · 82d
Cleared Dec 12, 2012
S4 SPINAL SYSTEM
K123352 · NKB
Orthopedic · 42d
Cleared Aug 04, 2011
AESCULAP SIBD XP SPINAL SYSTEM
K111122 · OVD
Orthopedic · 105d
Cleared Dec 02, 2010
LAMINOPLASY PLATING SYSTEM
K103284 · NQW
Orthopedic · 27d
Cleared Jul 20, 2010
AESCULAP IMPLANT SYSTEMS SIBD SPINAL SYSTEM
K100802 · OVD
Orthopedic · 120d
Cleared Sep 22, 2009
EXCIA TOTAL HIP SYSTEM M AN ML FEMORAL STEM
K092143 · MEH
Orthopedic · 69d
Cleared Jul 02, 2009
MILI (MINIMALLY INVASIVE LUMBAR IMPLANT) SYSTEM
K083004 · NKB
Orthopedic · 267d
Cleared Mar 04, 2009
AESCULAP CESPACE PEEK INTERVERTEBRAL BODY FUSION SYSTEM
K083311 · ODP
Orthopedic · 114d
Cleared Jan 15, 2009
MODIFICATION TO: METHA HIP SYSTEM
K083495 · LZO
Orthopedic · 51d
Cleared Nov 20, 2008
BIOLOX DELTA CERAMIC FEMORAL HEAD
K082991 · LZO
Orthopedic · 44d
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