Medical Device Manufacturer · US , Jacksonville , FL

Spine Next America Corporation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004

Recent clearances: FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 5, FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 1, 2, 3 AND 4

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Spine Next America Corporation Orthopedic ✕

2 devices

1-2 of 2

Cleared Dec 29, 2004

FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 5

Orthopedic · 90d

Cleared Dec 29, 2004

FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 1, 2, 3 AND 4

Orthopedic · 96d