X STOP INTERSPINOUS PROCESS DECOMPRESSION SYSTEM MANUFACTURED BY KYPHON, INC.

ShareThis

This company has been viewed 459 times within the past 60 days.

This product has been viewed: 355 times.

Request for Information Form	Contact Information
Company Name	KYPHON, INC.
Address	1221 CROSSMAN AVE.
City, State, Zip	SUNNYVALE, CA 94089
Country	US
FDA Owner/Operator Phone	408-548-6500
FDA Medical Specialty Code	OR - Orthopedic
FDA Product Code	NQO
FDA Classification Name	PROSTHESIS, SPINOUS PROCESS SPACER/PLATE
FDA Device Classification Code	Premarket Approval
FDA Regulation Number	NULL
FDA Common Generic Name	X STOP INTERSPINOUS PROCESS DECOMPRESSION SYSTEM
FDA Proprietary Device Name	X STOP INTERSPINOUS PROCESS DECOMPRESSION SYSTEM
FDA Owner / Operator Number	9034010
FDA Owner / Operator Name	KYPHON, INC.
FDA Establishment Registration Number	2953769
FDA Registered Establishment Name	KYPHON, INC.
FDA Operation Code(s)	MM - Manufacturer MR - Remanufacturer MS - Specification Developer RR - Repackager/Relabeller
FDA Listing Date	02-15-07
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A

Our records indicate that the following medical device companyies may manufacture a similar device.

	Company Name / Address / Phone	Proprietary Device Name	Common Generic Device Name
1	ST. FRANCIS MEDICAL TECHNOLOGIES, INC. 1201 MARINA VILLAGE PARKWAY SUITE 200 ALAMEDA, CA 94501 US 408-548-6500 / 408-548-6660	X STOP INTERSPINOUS PROCESS DECOMPRESSION SYSTEM	X STOP INTERSPINOUS PROCESS DECOMPRESSION SYSTEM