FDA 510(k)

STGC

K-Number: K121176 · 2012-08-17

Decision Date2012-08-17

Product CodeMQP

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

STGC is the device name listed in this FDA 510(k) record. The listed applicant is Cardinal Spine, LLC. It received FDA 510(k) clearance on 2012-08-17 under 510(k) number K121176. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STGC?

STGC is a medical device that received FDA 510(k) clearance on 2012-08-17. The listed applicant is Cardinal Spine, LLC. The 510(k) number is K121176.

When did STGC receive FDA 510(k) clearance?

STGC received FDA 510(k) clearance on 2012-08-17, under 510(k) number K121176.

Who is the listed applicant for STGC?

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

What is the FDA product code for STGC?

The FDA product code for STGC is MQP.

Other records listing Cardinal Spine, 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.

K152568C-VBR K100698STCC

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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.