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Spinal Devices, LLC

United StatesFDA applicant, unverified

Devices
2

Catalogue2

Newest first, rows 1-2 of 2

  • Tiger Discectomy Device Ref K081240

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Phenix Cervical Interbody Device Ref K083167

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Spinal Devices, LLC have in the registry?

The registry currently lists 2 devices for Spinal Devices, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Spinal Devices, LLC's devices?

Among its 2 most recently registered devices, Spinal Devices, LLC has devices listed in FDA 510(k) (2 devices).

What risk classes do Spinal Devices, LLC's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Spinal Devices, LLC's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Spinal Devices, LLC in the registry?

The most recently registered devices listed for Spinal Devices, LLC include TIGER DISCECTOMY DEVICE and PHENIX CERVICAL INTERBODY DEVICE.

Generated automatically from registry data and not verified by a human reviewer.