GANNET®— 510(k) K262184
Substantially EquivalentBAAT Medical Products B.V.
FDA 510(k) clearance K262184 for GANNET®, Substantially Equivalent on 2026-10-22. Applicant: BAAT Medical Products B.V.. Device class: 2.
Clearance details
- Applicant
- BAAT Medical Products B.V.
- Product code
- Product code JDO
- Device class
- Class 2
- Regulation
- 21 CFR 888.3030
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hengelo, NL
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More clearances from BAAT Medical Products B.V.
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