Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech
United StatesFDA applicant, unverified
- Devices
- 2
What Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech makes
Pioneer Surgical Technology, Inc. manufactures orthopedic fixation devices, including the DVR® Crosslock Wrist Spanning Plate for wrist stabilization and the CODA™ Anterior Cervical Plate System for spinal support in cervical spine surgeries.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
DVR® Crosslock Wrist Spanning Plate (131849181) Ref K220244
Regimes: 510(k) Registry: 510(k)CODA™ Anterior Cervical Plate System Ref K230993
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech have in the registry?
The registry currently lists 2 devices for Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech's devices?
Among its 2 most recently registered devices, Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech has devices listed in FDA 510(k) (2 devices).
What risk classes do Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech in the registry?
The most recently registered devices listed for Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech include DVR® Crosslock Wrist Spanning Plate (131849181) and CODA™ Anterior Cervical Plate System.