FDA 510(k)

Talee, Talee PostOp

K-Number: K241957 · 2024-08-30

Decision Date2024-08-30

Product CodeMVA

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Talee, Talee PostOp is the device name listed in this FDA 510(k) record. The listed applicant is Invent Medical USA, LLC. It received FDA 510(k) clearance on 2024-08-30 under 510(k) number K241957. 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 2024-08-30. The listed applicant is Invent Medical USA, LLC. The 510(k) number is K241957.

When did Talee, Talee PostOp receive FDA 510(k) clearance?

Talee, Talee PostOp received FDA 510(k) clearance on 2024-08-30, under 510(k) number K241957.

Who is the listed applicant for Talee, Talee PostOp?

The FDA 510(k) record lists Invent Medical USA, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Talee, Talee PostOp?

The FDA product code for Talee, Talee PostOp is MVA.

Other records listing Invent Medical USA, 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.

K230444Talee, Talee PostOp K220681Talee, Talee PostOP

Related Devices (Code: MVA)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.