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FDA 510(k)

SAVANNAH TECHNOLOGIES SPINAL SYSTEM

K-Number: K113755 · 2012-02-01

ApplicantSavannah Technologies, LLC
Decision Date2012-02-01
Product CodeMNI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SAVANNAH TECHNOLOGIES SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Savannah Technologies, LLC. It received FDA 510(k) clearance on 2012-02-01 under 510(k) number K113755. The device is classified under product code MNI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAVANNAH TECHNOLOGIES SPINAL SYSTEM?

SAVANNAH TECHNOLOGIES SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2012-02-01. The listed applicant is Savannah Technologies, LLC. The 510(k) number is K113755.

When did SAVANNAH TECHNOLOGIES SPINAL SYSTEM receive FDA 510(k) clearance?

SAVANNAH TECHNOLOGIES SPINAL SYSTEM received FDA 510(k) clearance on 2012-02-01, under 510(k) number K113755.

Who is the listed applicant for SAVANNAH TECHNOLOGIES SPINAL SYSTEM?

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

What is the FDA product code for SAVANNAH TECHNOLOGIES SPINAL SYSTEM?

The FDA product code for SAVANNAH TECHNOLOGIES SPINAL SYSTEM is MNI.

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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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