FIXED, VARIABLE & CORPECTOMY CERVICAL PLATE SYSTEM
K-Number: K073708 · 2008-06-03
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Device Summary
Frequently Asked Questions
What is the FIXED, VARIABLE & CORPECTOMY CERVICAL PLATE SYSTEM?
FIXED, VARIABLE & CORPECTOMY CERVICAL PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2008-06-03. The listed applicant is Precision Surgery , Ltd.. The 510(k) number is K073708.
When did FIXED, VARIABLE & CORPECTOMY CERVICAL PLATE SYSTEM receive FDA 510(k) clearance?
FIXED, VARIABLE & CORPECTOMY CERVICAL PLATE SYSTEM received FDA 510(k) clearance on 2008-06-03, under 510(k) number K073708.
Who is the listed applicant for FIXED, VARIABLE & CORPECTOMY CERVICAL PLATE SYSTEM?
The FDA 510(k) record lists Precision Surgery , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FIXED, VARIABLE & CORPECTOMY CERVICAL PLATE SYSTEM?
The FDA product code for FIXED, VARIABLE & CORPECTOMY 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 Precision Surgery , 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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