Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SeaSpine Vu cPOD, Zuma-C, Complete Cervical

K-Number: K172926 · 2017-12-21

Decision Date2017-12-21
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SeaSpine Vu cPOD, Zuma-C, Complete Cervical is the device name listed in this FDA 510(k) record. The listed applicant is SeaSpine Orthopedics Corporation. It received FDA 510(k) clearance on 2017-12-21 under 510(k) 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. The listed applicant is SeaSpine Orthopedics Corporation. The 510(k) number is K172926.

When did SeaSpine Vu cPOD, Zuma-C, Complete Cervical receive FDA 510(k) clearance?

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

Who is the listed applicant for SeaSpine Vu cPOD, Zuma-C, Complete Cervical?

The FDA 510(k) record lists SeaSpine Orthopedics Corporation as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing SeaSpine Orthopedics Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 67 devices →

Related Devices (Code: ODP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.