Medical Device Manufacturer · US , Clifton , NJ

Accelerated Innovation, LLC - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2008
7
Total
7
Cleared
0
Denied

Accelerated Innovation, LLC has 7 FDA 510(k) cleared medical devices. Based in Clifton, US.

Historical record: 7 cleared submissions from 2008 to 2008. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Accelerated Innovation, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Accelerated Innovation, LLC
7 devices
1-7 of 7
Cleared Oct 17, 2008
ACCIN TOTAL KNEE SYSTEM
K081127 · JWH
Orthopedic · 179d
Cleared Jul 08, 2008
ACCIN BIPOLAR HEAD SYSTEM
K080647 · KWY
Orthopedic · 123d
Cleared Jun 02, 2008
ACCIN UNIPOLAR HEAD SYSTEM
K080539 · JDI
Orthopedic · 96d
Cleared Feb 29, 2008
ACCIN PATELLOFEMORAL SYSTEM
K073120 · KRR
Orthopedic · 116d
Cleared Feb 04, 2008
ACCIN PEDICLE SCREW SYSTEM
K073531 · MNH
Orthopedic · 49d
Cleared Jan 31, 2008
ACCIN ANTERIOR CERVICAL PLATE SYSTEM
K073530 · KWQ
Orthopedic · 45d
Cleared Jan 10, 2008
ACCIN HIP SYSTEM
K073068 · LPH
Orthopedic · 72d
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