Talee, Talee PostOp
K-Number: K230444 · 2023-06-22
ApplicantInvent Medical USA, LLC
Decision Date2023-06-22
Product CodeMVA
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Talee, Talee PostOp is a medical device manufactured by Invent Medical USA, LLC. It received FDA 510(k) clearance on 2023-06-22 under approval number K230444. The device is classified under product code MVA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Talee, Talee PostOp?
Talee, Talee PostOp is a medical device that received FDA 510(k) clearance on 2023-06-22. It is manufactured by Invent Medical USA, LLC. The 510(k) number is K230444.
When was Talee, Talee PostOp approved by the FDA?
Talee, Talee PostOp received FDA 510(k) clearance on 2023-06-22, under approval number K230444.
What company makes Talee, Talee PostOp?
Talee, Talee PostOp is manufactured by Invent Medical USA, LLC.
What is the FDA product code for Talee, Talee PostOp?
The FDA product code for Talee, Talee PostOp is MVA.
Other Devices by Invent Medical USA, LLC
Related Devices (Code: MVA)
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.