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FDA 510(k)

GPS TM, G SURGICAL ANTERIOR CERVICAL PLATE SYSTEM +

K-Number: K103070 · 2011-01-12

Decision Date2011-01-12
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GPS TM, G SURGICAL ANTERIOR CERVICAL PLATE SYSTEM + is the device name listed in this FDA 510(k) record. The listed applicant is G Surgical Co., Ltd.. It received FDA 510(k) clearance on 2011-01-12 under 510(k) number K103070. 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 GPS TM, G SURGICAL ANTERIOR CERVICAL PLATE SYSTEM +?

GPS TM, G SURGICAL ANTERIOR CERVICAL PLATE SYSTEM + is a medical device that received FDA 510(k) clearance on 2011-01-12. The listed applicant is G Surgical Co., Ltd.. The 510(k) number is K103070.

When did GPS TM, G SURGICAL ANTERIOR CERVICAL PLATE SYSTEM + receive FDA 510(k) clearance?

GPS TM, G SURGICAL ANTERIOR CERVICAL PLATE SYSTEM + received FDA 510(k) clearance on 2011-01-12, under 510(k) number K103070.

Who is the listed applicant for GPS TM, G SURGICAL ANTERIOR CERVICAL PLATE SYSTEM +?

The FDA 510(k) record lists G Surgical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GPS TM, G SURGICAL ANTERIOR CERVICAL PLATE SYSTEM +?

The FDA product code for GPS TM, G SURGICAL ANTERIOR CERVICAL PLATE SYSTEM + is KWQ.

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 G Surgical Co., Ltd. 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: KWQ)

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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