SYNTHES SCALLOPED DISTAL TIBIA PLATE— 510(k) K001793
Substantially EquivalentSynthes (Usa)
FDA 510(k) clearance K001793 for SYNTHES SCALLOPED DISTAL TIBIA PLATE, Substantially Equivalent on 2000-08-17. Applicant: Synthes (Usa).
Clearance details
- Applicant
- Synthes (Usa)
- Product code
- Code LXT
- Advisory panel
- Orthopedic
- 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.