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FDA 510(k)

Coveris Cervical Cage System

K-Number: K170550 · 2017-07-13

Decision Date2017-07-13
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Coveris Cervical Cage System is a medical device manufactured by Camber Spine Technologies. It received FDA 510(k) clearance on 2017-07-13 under approval number K170550. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Coveris Cervical Cage System?

Coveris Cervical Cage System is a medical device that received FDA 510(k) clearance on 2017-07-13. It is manufactured by Camber Spine Technologies. The 510(k) number is K170550.

When was Coveris Cervical Cage System approved by the FDA?

Coveris Cervical Cage System received FDA 510(k) clearance on 2017-07-13, under approval number K170550.

What company makes Coveris Cervical Cage System?

Coveris Cervical Cage System is manufactured by Camber Spine Technologies.

What is the FDA product code for Coveris Cervical Cage System?

The FDA product code for Coveris Cervical Cage System is ODP.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.