Spine-Tech, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Spine-Tech Laparoscopic Instrumentation System Ref K940913
Regimes: 510(k) Registry: 510(k)Spine-Tech Bone Harvester Ref K970040
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Spine-Tech Silhouette Spinal Fixation System Ref K980288
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spine-Tech, Inc. have in the registry?
The registry currently lists 4 devices for Spine-Tech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spine-Tech, Inc.'s devices?
Among its 4 most recently registered devices, Spine-Tech, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Spine-Tech, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Spine-Tech, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spine-Tech, Inc. in the registry?
The most recently registered devices listed for Spine-Tech, Inc. include SPINE-TECH LAPAROSCOPIC INSTRUMENTATION SYSTEM, SPINE-TECH BONE HARVESTER, SPINE-TECH MODIFIED LAPAROSCOPIC SPINAL FUSION INSTRUMENT SYSTEM and SPINE-TECH SILHOUETTE SPINAL FIXATION SYSTEM.