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FDA 510(k)

VERTEVIEW ANTERIOR CERVICAL PLATE SYSTEM

K-Number: K050588 · 2005-04-21

ApplicantInnovative Spinal Design, LLC
Decision Date2005-04-21
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VERTEVIEW ANTERIOR CERVICAL PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Spinal Design, LLC. It received FDA 510(k) clearance on 2005-04-21 under 510(k) number K050588. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERTEVIEW ANTERIOR CERVICAL PLATE SYSTEM?

VERTEVIEW ANTERIOR CERVICAL PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2005-04-21. The listed applicant is Innovative Spinal Design, LLC. The 510(k) number is K050588.

When did VERTEVIEW ANTERIOR CERVICAL PLATE SYSTEM receive FDA 510(k) clearance?

VERTEVIEW ANTERIOR CERVICAL PLATE SYSTEM received FDA 510(k) clearance on 2005-04-21, under 510(k) number K050588.

Who is the listed applicant for VERTEVIEW ANTERIOR CERVICAL PLATE SYSTEM?

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

What is the FDA product code for VERTEVIEW ANTERIOR CERVICAL PLATE SYSTEM?

The FDA product code for VERTEVIEW ANTERIOR CERVICAL PLATE SYSTEM is KWQ.

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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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