Rivarp Medical Private Limited
IndiaFDA applicant, unverified
- Devices
- 1
What Rivarp Medical Private Limited makes
Rivarp Medical Private Limited manufactures the Kentrospine PSS Pedicle Screw System, a spinal fixation device used for orthopedic surgical procedures to stabilize the spine.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the US regulatory system.
Catalogue
Kentrospine PSS Pedicle Screw System Ref K220486
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rivarp Medical Private Limited have in the registry?
The registry currently lists 1 device for Rivarp Medical Private Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rivarp Medical Private Limited's devices?
Among its 1 most recently registered device, Rivarp Medical Private Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Rivarp Medical Private Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Rivarp Medical Private Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rivarp Medical Private Limited in the registry?
The most recently registered devices listed for Rivarp Medical Private Limited include Kentrospine PSS Pedicle Screw System.