Talee, Talee PostOp— 510(k) K241957
Substantially EquivalentInvent Medical USA, LLC
FDA 510(k) clearance K241957 for Talee, Talee PostOp, Substantially Equivalent on 2024-08-30. Applicant: Invent Medical USA, LLC. Device class: 2.
Clearance details
- Applicant
- Invent Medical USA, LLC
- Product code
- Code MVA
- Device class
- Class 2
- Regulation
- 21 CFR 882.5970
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Warminster, PA, US
Recent devices under product code MVA
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