Dynamic TiBase; TRI Screws
K-Number: K241170 · 2024-10-21
ApplicantTalladium España, SL
Decision Date2024-10-21
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Dynamic TiBase; TRI Screws is a medical device manufactured by Talladium España, SL. It received FDA 510(k) clearance on 2024-10-21 under approval number K241170. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Dynamic TiBase; TRI Screws?
Dynamic TiBase; TRI Screws is a medical device that received FDA 510(k) clearance on 2024-10-21. It is manufactured by Talladium España, SL. The 510(k) number is K241170.
When was Dynamic TiBase; TRI Screws approved by the FDA?
Dynamic TiBase; TRI Screws received FDA 510(k) clearance on 2024-10-21, under approval number K241170.
What company makes Dynamic TiBase; TRI Screws?
Dynamic TiBase; TRI Screws is manufactured by Talladium España, SL.
What is the FDA product code for Dynamic TiBase; TRI Screws?
The FDA product code for Dynamic TiBase; TRI Screws is NHA.
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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.