MODIFICATION TO PREMIER III PHASED ARRAY CTL SPINE COIL— 510(k) K031056

Substantially Equivalent

Usa Instruments, Inc.

FDA 510(k) clearance K031056 for MODIFICATION TO PREMIER III PHASED ARRAY CTL SPINE COIL, Substantially Equivalent on 2003-05-08. Applicant: Usa Instruments, Inc..

Clearance details

Applicant: Usa Instruments, Inc.
Product code: Code MOS
Advisory panel: Radiology
Date received: 2003-04-03
Decision date: 2003-05-08
Decision: Substantially Equivalent
Clearance type: Special
Location: Aurora, OH, US

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