KYPHON ELEMENT™ Balloon Kyphoplasty System

GUDID 00643169582231

BONE ACCESS TOOLS T25R VALUE BONE ACCESS

MEDTRONIC SOFAMOR DANEK, INC.

Bone access cannula Bone access cannula
Primary Device ID00643169582231
NIH Device Record Keyef1fefd9-eda9-414b-ab1f-033a3d34a966
Commercial Distribution StatusIn Commercial Distribution
Brand NameKYPHON ELEMENT™ Balloon Kyphoplasty System
Version Model NumberT25R
Company DUNS830350380
Company NameMEDTRONIC SOFAMOR DANEK, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100643169582231 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-10-14

On-Brand Devices [KYPHON ELEMENT™ Balloon Kyphoplasty System]

00643169582231BONE ACCESS TOOLS T25R VALUE BONE ACCESS
00643169582248BONE FILLER DEVICE F25R 3 VALUE BFD
20643169842735BONE FILLER 7480703T BFD SIZE 3
00643169582224INFLATION SYRINGE A25R VALUE SYRINGE

Trademark Results [KYPHON ELEMENT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
KYPHON ELEMENT
KYPHON ELEMENT
86559466 not registered Dead/Abandoned
Kyphon Sarl
2015-03-10

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.