STCC
K-Number: K100698 · 2011-03-14
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Device Summary
Frequently Asked Questions
What is the STCC?
STCC is a medical device that received FDA 510(k) clearance on 2011-03-14. The listed applicant is Cardinal Spine, LLC. The 510(k) number is K100698.
When did STCC receive FDA 510(k) clearance?
STCC received FDA 510(k) clearance on 2011-03-14, under 510(k) number K100698.
Who is the listed applicant for STCC?
The FDA 510(k) record lists Cardinal Spine, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STCC?
The FDA product code for STCC is ODP.
Other records listing Cardinal Spine, LLC 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: ODP)
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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