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FDA 510(k)

SeaSpine Vu cPOD, Zuma-C, Complete Cervical

K-Number: K172926 · 2017-12-21

ApplicantSeaSpine Orthopedics Corporation
Decision Date2017-12-21
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SeaSpine Vu cPOD, Zuma-C, Complete Cervical is a medical device manufactured by SeaSpine Orthopedics Corporation. It received FDA 510(k) clearance on 2017-12-21 under approval number K172926. 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 SeaSpine Vu cPOD, Zuma-C, Complete Cervical?

SeaSpine Vu cPOD, Zuma-C, Complete Cervical is a medical device that received FDA 510(k) clearance on 2017-12-21. It is manufactured by SeaSpine Orthopedics Corporation. The 510(k) number is K172926.

When was SeaSpine Vu cPOD, Zuma-C, Complete Cervical approved by the FDA?

SeaSpine Vu cPOD, Zuma-C, Complete Cervical received FDA 510(k) clearance on 2017-12-21, under approval number K172926.

What company makes SeaSpine Vu cPOD, Zuma-C, Complete Cervical?

SeaSpine Vu cPOD, Zuma-C, Complete Cervical is manufactured by SeaSpine Orthopedics Corporation.

What is the FDA product code for SeaSpine Vu cPOD, Zuma-C, Complete Cervical?

The FDA product code for SeaSpine Vu cPOD, Zuma-C, Complete Cervical is ODP.

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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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