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FDA 510(k)

SPIRA-C Open Matrix Cervical Interbody

K-Number: K172446 · 2017-11-07

ApplicantCamber Spine Technologies
Decision Date2017-11-07
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SPIRA-C Open Matrix Cervical Interbody is a medical device manufactured by Camber Spine Technologies. It received FDA 510(k) clearance on 2017-11-07 under approval number K172446. 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 SPIRA-C Open Matrix Cervical Interbody?

SPIRA-C Open Matrix Cervical Interbody is a medical device that received FDA 510(k) clearance on 2017-11-07. It is manufactured by Camber Spine Technologies. The 510(k) number is K172446.

When was SPIRA-C Open Matrix Cervical Interbody approved by the FDA?

SPIRA-C Open Matrix Cervical Interbody received FDA 510(k) clearance on 2017-11-07, under approval number K172446.

What company makes SPIRA-C Open Matrix Cervical Interbody?

SPIRA-C Open Matrix Cervical Interbody is manufactured by Camber Spine Technologies.

What is the FDA product code for SPIRA-C Open Matrix Cervical Interbody?

The FDA product code for SPIRA-C Open Matrix Cervical Interbody is ODP.

Related Clinical Trials

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Other Devices by Camber Spine Technologies

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Related Devices (Code: ODP)

K161127The Small PLATEAU (PLATEAU-C) Spacer SystemLife Spine, Inc. K162003IMSE Cervical CageThe Institute of Musculoskeletal Science & Education K160222OIC Cervical PEEK SpacerThe Orthopaedic Implant Company K161809ShurFit CpTi-HA ACIF Interbody Fusion SystemPrecision Spine, Inc. K162220DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) CageDio Medical Co., Ltd. K161649Virtu C Spinal Implant SystemMet 1 Technologies, LLC

Official Source

View on FDA Database →

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

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