Lsk Biopartners, Inc.
Country not established
- Devices
- 1
What Lsk Biopartners, Inc. makes
Lsk Biopartners, Inc. manufactures the MEGA 5.5 SPINE SYSTEM, a spinal fixation device designed for surgical applications in the lumbar spine region.
The company’s portfolio is regulated under FDA’s Class II device classification, with the MEGA 5.5 SPINE SYSTEM authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Mega 5.5 Spine System Ref K123476
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lsk Biopartners, Inc. have in the registry?
The registry currently lists 1 device for Lsk Biopartners, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lsk Biopartners, Inc.'s devices?
Among its 1 most recently registered device, Lsk Biopartners, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Lsk Biopartners, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lsk Biopartners, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lsk Biopartners, Inc. in the registry?
The most recently registered devices listed for Lsk Biopartners, Inc. include MEGA 5.5 SPINE SYSTEM.