NUVASIVE OCT SYSTEM
K-Number: K071435 · 2007-08-06
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Device Summary
Frequently Asked Questions
What is the NUVASIVE OCT SYSTEM?
NUVASIVE OCT SYSTEM is a medical device that received FDA 510(k) clearance on 2007-08-06. The listed applicant is Nuvasive, Inc.. The 510(k) number is K071435.
When did NUVASIVE OCT SYSTEM receive FDA 510(k) clearance?
NUVASIVE OCT SYSTEM received FDA 510(k) clearance on 2007-08-06, under 510(k) number K071435.
Who is the listed applicant for NUVASIVE OCT SYSTEM?
The FDA 510(k) record lists Nuvasive, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NUVASIVE OCT SYSTEM?
The FDA product code for NUVASIVE OCT SYSTEM is MNI.
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 Nuvasive, Inc. 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: MNI)
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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