Ti-Diagon Oblique TLIF
K-Number: K172064 · 2017-09-15
ApplicantCamber Spine Technologies
Decision Date2017-09-15
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Ti-Diagon Oblique TLIF is a medical device manufactured by Camber Spine Technologies. It received FDA 510(k) clearance on 2017-09-15 under approval number K172064. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Ti-Diagon Oblique TLIF?
Ti-Diagon Oblique TLIF is a medical device that received FDA 510(k) clearance on 2017-09-15. It is manufactured by Camber Spine Technologies. The 510(k) number is K172064.
When was Ti-Diagon Oblique TLIF approved by the FDA?
Ti-Diagon Oblique TLIF received FDA 510(k) clearance on 2017-09-15, under approval number K172064.
What company makes Ti-Diagon Oblique TLIF?
Ti-Diagon Oblique TLIF is manufactured by Camber Spine Technologies.
What is the FDA product code for Ti-Diagon Oblique TLIF?
The FDA product code for Ti-Diagon Oblique TLIF is MAX.
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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.