HAVEN Laminoplasty System, CANOPY® Laminoplasty Fixation System— 510(k) K171413
Substantially EquivalentGlobus Medical, Inc.
FDA 510(k) clearance K171413 for HAVEN Laminoplasty System, CANOPY® Laminoplasty Fixation System, Substantially Equivalent on 2017-07-14. Applicant: Globus Medical, Inc..
Clearance details
- Applicant
- Globus Medical, Inc.
- Product code
- Code NQW
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Audubon, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.