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FDA 510(k)

DAYTONA ANTERIOR CERVICAL CAGE

K-Number: K110733 · 2011-08-25

ApplicantSpinenet, LLC
Decision Date2011-08-25
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DAYTONA ANTERIOR CERVICAL CAGE is the device name listed in this FDA 510(k) record. The listed applicant is Spinenet, LLC. It received FDA 510(k) clearance on 2011-08-25 under 510(k) number K110733. 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 DAYTONA ANTERIOR CERVICAL CAGE?

DAYTONA ANTERIOR CERVICAL CAGE is a medical device that received FDA 510(k) clearance on 2011-08-25. The listed applicant is Spinenet, LLC. The 510(k) number is K110733.

When did DAYTONA ANTERIOR CERVICAL CAGE receive FDA 510(k) clearance?

DAYTONA ANTERIOR CERVICAL CAGE received FDA 510(k) clearance on 2011-08-25, under 510(k) number K110733.

Who is the listed applicant for DAYTONA ANTERIOR CERVICAL CAGE?

The FDA 510(k) record lists Spinenet, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAYTONA ANTERIOR CERVICAL CAGE?

The FDA product code for DAYTONA ANTERIOR CERVICAL CAGE is ODP.

Related Clinical Trials

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.

Other records listing Spinenet, LLC 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.

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

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

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