Sirakoss, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Sirakoss, Ltd. makes
Sirakoss, Ltd. manufactures the Osteo3 ZP Putty, a bone void filler designed for use in orthopedic and spinal surgeries to fill gaps or defects in bone structure during procedures.
The Osteo3 ZP Putty is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Osteo3 ZP Putty Ref K193075
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sirakoss, Ltd. have in the registry?
The registry currently lists 1 device for Sirakoss, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sirakoss, Ltd.'s devices?
Among its 1 most recently registered device, Sirakoss, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Sirakoss, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sirakoss, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sirakoss, Ltd. in the registry?
The most recently registered devices listed for Sirakoss, Ltd. include Osteo3 ZP Putty.