PREMIER 7000 CTL SPINE COIL— 510(k) K980157
Substantially EquivalentUsa Instruments, Inc.
FDA 510(k) clearance K980157 for PREMIER 7000 CTL SPINE COIL, Substantially Equivalent on 1998-04-13. Applicant: Usa Instruments, Inc..
Clearance details
- Applicant
- Usa Instruments, Inc.
- Product code
- Code MOS
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Highland Heights, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.