Medical Device Manufacturer · US , Buffalo , NY

Praesidia S.R.L. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2006

Recent clearances: FLEXIGRIP STERNAL CLOSURE SYSTEM, MODEL FG0200 THROUGH FG0400 (NONE SIZES)

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Praesidia S.R.L. Orthopedic ✕

1 devices

1-1 of 1

Cleared Dec 27, 2006

FLEXIGRIP STERNAL CLOSURE SYSTEM, MODEL FG0200 THROUGH FG0400 (NONE SIZES)

Orthopedic · 86d