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FDA 510(k)

Tritanium C Anterior Cervical Cage

K-Number: K171496 · 2017-09-06

ApplicantStryker Spine
Decision Date2017-09-06
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Tritanium C Anterior Cervical Cage is a medical device manufactured by Stryker Spine. It received FDA 510(k) clearance on 2017-09-06 under approval number K171496. 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 Tritanium C Anterior Cervical Cage?

Tritanium C Anterior Cervical Cage is a medical device that received FDA 510(k) clearance on 2017-09-06. It is manufactured by Stryker Spine. The 510(k) number is K171496.

When was Tritanium C Anterior Cervical Cage approved by the FDA?

Tritanium C Anterior Cervical Cage received FDA 510(k) clearance on 2017-09-06, under approval number K171496.

What company makes Tritanium C Anterior Cervical Cage?

Tritanium C Anterior Cervical Cage is manufactured by Stryker Spine.

What is the FDA product code for Tritanium C Anterior Cervical Cage?

The FDA product code for Tritanium C Anterior Cervical Cage is ODP.

Related Clinical Trials

NCT06938607 Post-operative Outcomes of Anterior Cervical Discectomy and Fusion Surgery With and Without Drain Placement NOT_YET_RECRUITING NCT04214535 Anterior Cervical Disectomy And Fusion Using The Tritanium® C Anterior Cervical Cage For One Or Two-Levels ACTIVE_NOT_RECRUITING

Other Devices by Stryker Spine

K161407Ascential IBD PEEKc Spacer K181014Tritanium PL Cage K183249Tritanium X PL Expandable Posterior Lumbar Cage, Tritanium X TL Expandable Curved Posterior Lumbar Cage K183071VLIFT-s Vertebral Body Replacement System K200666Stryker Xia 3 Power Adaptor K203205Navigated Spine Instruments

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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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