MFG-05— 510(k) K230780
Substantially EquivalentZimmer Medizinsysteme GmbH
FDA 510(k) clearance K230780 for MFG-05, Substantially Equivalent on 2023-10-05. Applicant: Zimmer Medizinsysteme GmbH. Device class: 2.
Clearance details
- Applicant
- Zimmer Medizinsysteme GmbH
- Product code
- Code KPI
- Device class
- Class 2
- Regulation
- 21 CFR 876.5320
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Neu-Elm, DE
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More clearances from Zimmer Medizinsysteme GmbH
view allData sourced from openFDA. This site is unofficial and independent of the FDA.