GPS TM, G SURGICAL ANTERIOR CERVICAL PLATE SYSTEM +
K-Number: K103070 · 2011-01-12
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Device Summary
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
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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