SYNTHES (USA) CHRONOS— 510(k) K041350
Substantially EquivalentSynthes (Usa)
FDA 510(k) clearance K041350 for SYNTHES (USA) CHRONOS, Substantially Equivalent on 2004-07-08. Applicant: Synthes (Usa).
Clearance details
- Applicant
- Synthes (Usa)
- Product code
- Code GXP
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Paoli, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.