Apollo Spine, Inc.
Also registered as Apollo Spine
United StatesFDA applicant, unverified
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Venus Facet Screw System Ref K120340
Regimes: 510(k) Registry: 510(k)Eclipse Vertebral Spacer System-Cervical Ref K101588
Regimes: 510(k) Registry: 510(k)Apollo Anterior Cervical Plate System Ref K082504
Regimes: 510(k) Registry: 510(k)Eclipse Vertebral Spacer System-Cervical Ref K120143
Regimes: 510(k) Registry: 510(k)Zenith Pedicle System Ref K102636
Regimes: 510(k) Registry: 510(k)Comet Anterior Cervical Plate System Ref K090751
Regimes: 510(k) Registry: 510(k)Eclipse Vertebral Spacer System-Lumbar Ref K102121
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Apollo Spine, Inc. have in the registry?
The registry currently lists 7 devices for Apollo Spine, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Apollo Spine, Inc.'s devices?
Among its 7 most recently registered devices, Apollo Spine, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Apollo Spine, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Apollo Spine, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Apollo Spine, Inc. in the registry?
The most recently registered devices listed for Apollo Spine, Inc. include VENUS FACET SCREW SYSTEM, ECLIPSE VERTEBRAL SPACER SYSTEM-CERVICAL, APOLLO ANTERIOR CERVICAL PLATE SYSTEM and ZENITH PEDICLE SYSTEM.