PROGENIX PLUS— 510(k) K081950
Substantially EquivalentMedtronic Sofamor Danek, Inc.
FDA 510(k) clearance K081950 for PROGENIX PLUS, Substantially Equivalent on 2008-07-18. Applicant: Medtronic Sofamor Danek, Inc.. Device class: 2.
Clearance details
- Applicant
- Medtronic Sofamor Danek, Inc.
- Product code
- Code NUN
- Device class
- Class 2
- Regulation
- 21 CFR 872.3930
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Memphis, TN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.