Surgicraft, Ltd.
Country not established
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Surgicraft Screw Fixation System Ref K080447
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Ransford Cervical Fixation System Ref K965221
Regimes: 510(k) Registry: 510(k)Stalif Tt Intervertebral Body Fusion System Ref K073109
Regimes: 510(k) Registry: 510(k)Surgicraft Surgical Mesh System Ref K072370
Regimes: 510(k) Registry: 510(k)Titanium Hartshill System Ref K991662
Regimes: 510(k) Registry: 510(k)Stalif Tt Ref K041617
Regimes: 510(k) Registry: 510(k)Stalif (Tm) C Ref K072415
Regimes: 510(k) Registry: 510(k)Stalif Tt Ref K051027
Regimes: 510(k) Registry: 510(k)The Bone Tie Ref K982719
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgicraft, Ltd. have in the registry?
The registry currently lists 10 devices for Surgicraft, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgicraft, Ltd.'s devices?
Among its 10 most recently registered devices, Surgicraft, Ltd. has devices listed in FDA 510(k) (10 devices).
What risk classes do Surgicraft, Ltd.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Surgicraft, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgicraft, Ltd. in the registry?
The most recently registered devices listed for Surgicraft, Ltd. include SURGICRAFT SCREW FIXATION SYSTEM, SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE, RANSFORD CERVICAL FIXATION SYSTEM and STALIF TT INTERVERTEBRAL BODY FUSION SYSTEM.