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FDA 510(k)

SAVANNAH LUMBAR PERCUTANEOUS STABILIZATION SYSTEM

K-Number: K072116 · 2008-03-20

ApplicantNeurospine Innovations and Solutions
Decision Date2008-03-20
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SAVANNAH LUMBAR PERCUTANEOUS STABILIZATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Neurospine Innovations and Solutions. It received FDA 510(k) clearance on 2008-03-20 under 510(k) number K072116. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAVANNAH LUMBAR PERCUTANEOUS STABILIZATION SYSTEM?

SAVANNAH LUMBAR PERCUTANEOUS STABILIZATION SYSTEM is a medical device that received FDA 510(k) clearance on 2008-03-20. The listed applicant is Neurospine Innovations and Solutions. The 510(k) number is K072116.

When did SAVANNAH LUMBAR PERCUTANEOUS STABILIZATION SYSTEM receive FDA 510(k) clearance?

SAVANNAH LUMBAR PERCUTANEOUS STABILIZATION SYSTEM received FDA 510(k) clearance on 2008-03-20, under 510(k) number K072116.

Who is the listed applicant for SAVANNAH LUMBAR PERCUTANEOUS STABILIZATION SYSTEM?

The FDA 510(k) record lists Neurospine Innovations and Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAVANNAH LUMBAR PERCUTANEOUS STABILIZATION SYSTEM?

The FDA product code for SAVANNAH LUMBAR PERCUTANEOUS STABILIZATION SYSTEM is NKB.

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Related Devices (Code: NKB)

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.

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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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