Medical Device Manufacturer · US , Minneapolis , MN

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

4 submissions · 2 cleared · Since 2002
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)
K033679 · MQV
Orthopedic · 226d
Cleared Mar 05, 2004
DYNESYS SPINAL SYSTEM
K031511 · NQP
Orthopedic · 296d
Cleared Oct 29, 2002
CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR
K022615 · JDK
Orthopedic · 83d
Cleared Sep 24, 2002
TRINICA SELECT ANTERIOR CERVICAL PLATE SYSTEM
K022344 · KWQ
Orthopedic · 67d
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