OCTAVE SPEEDER SPINE— 510(k) K121911
Substantially EquivalentToshiba Medical Systems Corporation, Japan
FDA 510(k) clearance K121911 for OCTAVE SPEEDER SPINE, Substantially Equivalent on 2012-08-17. Applicant: Toshiba Medical Systems Corporation, Japan. Device class: 2.
Clearance details
- Applicant
- Toshiba Medical Systems Corporation, Japan
- Product code
- Code MOS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1000
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Tustin, CA, US
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More clearances from Toshiba Medical Systems Corporation, Japan
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