Centerpulse Spine-Tech, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Centerpulse Spine-Tech, Inc. makes
Centerpulse Spine-Tech, Inc. manufactures spinal systems including the DYNESYS SPINAL SYSTEM and TRINICA SELECT ANTERIOR CERVICAL PLATE SYSTEM, as well as bone void fillers like COPSIOS BONE VOID FILLER (BVF) and a CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR.
The company's devices are classified as Class II and listed in the FDA 510(k) registry. Centerpulse Spine-Tech, Inc. is based in the US.
Catalogue
Dynesys Spinal System Ref K031511
Regimes: 510(k) Registry: 510(k)Copsios Bone Void Filler (Bvf) Ref K033679
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Trinica Select Anterior Cervical Plate System Ref K022344
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Centerpulse Spine-Tech, Inc. have in the registry?
The registry currently lists 4 devices for Centerpulse Spine-Tech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Centerpulse Spine-Tech, Inc.'s devices?
Among its 4 most recently registered devices, Centerpulse Spine-Tech, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Centerpulse Spine-Tech, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Centerpulse Spine-Tech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Centerpulse Spine-Tech, Inc. in the registry?
The most recently registered devices listed for Centerpulse Spine-Tech, Inc. include DYNESYS SPINAL SYSTEM, COPSIOS BONE VOID FILLER (BVF), CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR and TRINICA SELECT ANTERIOR CERVICAL PLATE SYSTEM.