Medical Device Manufacturer · US , Minneapolis , MN

Centerpulse Spine-Tech, Inc. - FDA 510(k) Cleared Devices

4 submissions · 2 cleared · Since 2002

Recent clearances: COPSIOS BONE VOID FILLER (BVF), DYNESYS SPINAL SYSTEM, CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR

View 4 510(k) Devices ↓

4

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Centerpulse Spine-Tech, Inc. Orthopedic ✕

4 devices

1-4 of 4

Cleared Jul 07, 2004

COPSIOS BONE VOID FILLER (BVF)

Orthopedic · 226d

Cleared Mar 05, 2004

DYNESYS SPINAL SYSTEM

Orthopedic · 296d

Cleared Oct 29, 2002

CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR

Orthopedic · 83d

Cleared Sep 24, 2002

TRINICA SELECT ANTERIOR CERVICAL PLATE SYSTEM

Orthopedic · 67d