SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL
K-Number: K161710 · 2017-06-29
Device Summary
Frequently Asked Questions
What is the SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL?
SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL is a medical device that received FDA 510(k) clearance on 2017-06-29. The listed applicant is Spinal Analytics & Geometrical Impant Co, LLC. The 510(k) number is K161710.
When did SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL receive FDA 510(k) clearance?
SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL received FDA 510(k) clearance on 2017-06-29, under 510(k) number K161710.
Who is the listed applicant for SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL?
The FDA 510(k) record lists Spinal Analytics & Geometrical Impant Co, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL?
The FDA product code for SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL is MAX.
Related Devices (Code: MAX)
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
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