Cmf Medicon Surgical, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Cmf Medicon Surgical, Inc. makes
Cmf Medicon Surgical, Inc. manufactures orthopedic fixation systems, including pedicle screw implants for spinal stabilization, expandable vertebral body replacement (VBR) devices for spinal fusion, and titanium-coated plating systems for bone integration in surgical procedures.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
MediRod Pedicle Screw System Ref K242764
Regimes: 510(k) Registry: 510(k)MediExpand TL Expandable VBR System Ref K190349
Regimes: 510(k) Registry: 510(k)Medicon Epiplating System Ref K241253
Regimes: 510(k) Registry: 510(k)MediExpand Cervical Expandable VBR System Ref K212126
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cmf Medicon Surgical, Inc. have in the registry?
The registry currently lists 4 devices for Cmf Medicon Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cmf Medicon Surgical, Inc.'s devices?
Among its 4 most recently registered devices, Cmf Medicon Surgical, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Cmf Medicon Surgical, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Cmf Medicon Surgical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cmf Medicon Surgical, Inc. in the registry?
The most recently registered devices listed for Cmf Medicon Surgical, Inc. include MediRod Pedicle Screw System, MediExpand TL Expandable VBR System, Medicon Epiplating System and MediExpand Cervical Expandable VBR System.