Talee, Talee PostOP— 510(k) K220681
Substantially EquivalentInvent Medical USA, LLC
FDA 510(k) clearance K220681 for Talee, Talee PostOP, Substantially Equivalent on 2022-09-22. 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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