SPINE & TRAUMA ICT
K-Number: K083310 · 2009-04-01
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Device Summary
Frequently Asked Questions
What is the SPINE & TRAUMA ICT?
SPINE & TRAUMA ICT is a medical device that received FDA 510(k) clearance on 2009-04-01. The listed applicant is Brainlab AG. The 510(k) number is K083310.
When did SPINE & TRAUMA ICT receive FDA 510(k) clearance?
SPINE & TRAUMA ICT received FDA 510(k) clearance on 2009-04-01, under 510(k) number K083310.
Who is the listed applicant for SPINE & TRAUMA ICT?
The FDA 510(k) record lists Brainlab AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPINE & TRAUMA ICT?
The FDA product code for SPINE & TRAUMA ICT is OLO.
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 Brainlab AG 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: OLO)
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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