Aesculap, Inc. - FDA 510(k) Cleared Devices
207
Total
201
Cleared
0
Denied
FDA 510(k) cleared devices by Aesculap, Inc. Orthopedic ✕
47 devices
Cleared
Mar 14, 2007
MODIFICATION TO S4 SPINAL SYSTEM
Orthopedic
216d
Cleared
Feb 09, 2007
S4 CERVICAL OCCIPITAL PLATE SPINAL SYSTEM
Orthopedic
207d
Cleared
Dec 27, 2006
AESCULAP STERNUMFIX STERNAL CLOSURE SYSTEM
Orthopedic
86d
Cleared
Nov 22, 2006
EXCIA TOTAL HIP SYSTEM 36MM CERAMIC HEAD
Orthopedic
75d
Cleared
Sep 14, 2006
AESCULAP PEEK VERTEBRAL BODY REPLACEMENT SYSTEM
Orthopedic
177d
Cleared
Aug 18, 2006
EXCIA
Orthopedic
63d
Cleared
Aug 02, 2006
EXCIA TOTAL HIP SYSTEM LATERAL OFFSET
Orthopedic
79d
Cleared
May 31, 2006
AESCULAP BIPOLAR ACETABULAR CUP
Orthopedic
76d
Cleared
May 26, 2006
EXCIA TOTAL HIP SYSTEM 12/14 TRUNNION WITH CERAMIC HEAD
Orthopedic
52d
Cleared
May 17, 2006
COLUMBUS ULTRA CONGRUENT (UC) TIBIAL INSERT/GLIDING SURFACE
Orthopedic
146d
Cleared
Mar 22, 2006
EXCIA TOTAL HIP SYSTEM WITH U-CAP
Orthopedic
29d
Cleared
Feb 06, 2006
COLUMBUS (CR) TOTAL KNEE SYSTEM
Orthopedic
63d
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