VIPER F2 FACET FIXATION SYSTEM— 510(k) K101762
Substantially EquivalentDepuy Spine, Inc.
FDA 510(k) clearance K101762 for VIPER F2 FACET FIXATION SYSTEM, Substantially Equivalent on 2010-11-15. Applicant: Depuy Spine, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Depuy Spine, Inc.
- Product code
- Code MRW
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Raynham, MA, US
Recent devices under product code MRW
view allMore clearances from Depuy Spine, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.