STAXX FX STRUCTURAL KYPHOPLASTY SYSTEM MANUFACTURED BY SPINE WAVE, INC.

Please Login or Create an Account Now.

This company has been viewed 426 times within the past 60 days.

This product has been viewed: 316 times.

Request for Information Form	Contact Information
Company Name	SPINE WAVE, INC.
Address	TWO ENTERPRISE DR. SUITE 302
City, State, Zip	SHELTON, CT 06484
Country	US
FDA Owner/Operator Phone	203-944-9494 340
FDA Medical Specialty Code	OR - Orthopedic
FDA Product Code	OBL
FDA Classification Name	CEMENT, BONE, PRE-FORMED, MODULAR, POLYMERIC, VERTEBROPLASTY
FDA Device Classification Code	Standards
FDA Regulation Number	888.3027
FDA Common Generic Name	KYPHOPLASTY SYSTEM
FDA Proprietary Device Name	STAXX FX STRUCTURAL KYPHOPLASTY SYSTEM
FDA Owner / Operator Number	9055730
FDA Owner / Operator Name	SPINE WAVE, INC.
FDA Establishment Registration Number	3004638600
FDA Registered Establishment Name	SPINE WAVE, INC.
FDA Operation Code(s)	MM - Manufacturer MS - Specification Developer
FDA Listing Date	07-18-07
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A