ULTRAZONIX SPINE MINIMAL-INVASIVE DISC SYSTEM— 510(k) K060346
Substantially EquivalentUltrazonix Dnt AB
FDA 510(k) clearance K060346 for ULTRAZONIX SPINE MINIMAL-INVASIVE DISC SYSTEM, Substantially Equivalent on 2006-12-22. Applicant: Ultrazonix Dnt AB. Device class: 2.
Clearance details
- Applicant
- Ultrazonix Dnt AB
- Product code
- Code NTB
- Device class
- Class 2
- Regulation
- 21 CFR 878.4400
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.