OCTAVE SPEEDER SPINE— 510(k) K121911

Substantially Equivalent

Toshiba 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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