Medical Device Manufacturer · US , Center Valley , PA

Aesculap Implant Systems - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2007

Recent clearances: VEGA KNEE SYSTEM, VEGA KNEE SYSTEM, ENDURO KNEE SYSTEM

View 7 510(k) Devices ↓
7
Total
7
Cleared
0
Denied

FDA 510(k) Regulatory Record - Aesculap Implant Systems Orthopedic ✕

7 devices
1-7 of 7
Cleared Mar 25, 2014
VEGA KNEE SYSTEM
K140452 · JWH
Orthopedic · 29d
Cleared Jul 27, 2012
VEGA KNEE SYSTEM
K121879 · JWH
Orthopedic · 29d
Cleared Dec 20, 2010
ENDURO KNEE SYSTEM
K101815 · KRO
Orthopedic · 173d
Cleared Jun 09, 2010
AESCULAP IMPLANT SYSTEMS S4 SPINAL SYSTEM
K100623 · NKB
Orthopedic · 97d
Cleared Apr 24, 2009
BIOLOX OPTION CERAMIC FEMORAL HEAD AND METHA XL HEADS
K090299 · LZO
Orthopedic · 77d
Cleared Apr 20, 2009
MODIFICATION TO: S4 SPINAL SYSTEM
K090657 · NKB
Orthopedic · 39d
Cleared Sep 20, 2007
S4 SPINAL SYSTEM
K071945 · NKB
Orthopedic · 69d
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