CD HORIZON® SOLERA® VOYAGER™ Spinal System

Primary DI
00763000216719
Brand
CD HORIZON® SOLERA® VOYAGER™ Spinal System
Company
MEDTRONIC SOFAMOR DANEK, INC.
Model
6550038
Device description
DRIVER 6550038 VOYAGER SAS DRIVER
Published
2020-12-31
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
HBEDRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HBEDrills, Burrs, Trephines & Accessories (Simple, Powered)Neurology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K201362000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K201362000CD Horizon™ Fenestrated Screw Set, CD Horizon™ Spinal System, Kyphon™ HV-R™ Bone CementMedtronic2020-08-19PML

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00763000216719PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00763000216719007630002167197630002167190763000216719

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic implantable material dispenser, reservoir-containingA non-powered, syringe-/pipette-like device intended to load orthopaedic cement and/or a bone void filling material (not included) within an included reservoir/barrel and dispense the material during surgery. It is not designed to accept a separate cartridge/syringe or prepare/mix the substance. It may be intended to be manually-operated or mounted in a powered unit that drives the piston down the syringe barrel. This is a single-use device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(800)633-8766Corporate.UDI@medtronic.com

Regulatory Flags#

DUNS number
830350380
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00199150081073Medtronic Reusable InstrumentsX04260042026-07-30
20763000211015Medtronic Reusable Instrument65501022022-10-16
20763000211039Medtronic Reusable Instrument65502022022-10-16
00763000311667KYPHON® Directional Bone Filler DeviceF04C2020-11-06
00763000311681KYPHON® EXPRESS™ Bone Filler DeviceF06A2020-11-06
00763000311698KYPHON® EXPRESS™ Directional Bone Filler DeviceF06B2020-11-06
0076300031183413 Ga TampVPT02A2020-11-06
00763000883478N/a7480757T2025-06-01
00763000883485N/a7480758T2025-06-01
00763000711993N/A65500422024-12-28
00763000712006N/A65500432024-12-28
00763000712013N/A65500442024-12-28
00763000712020n/a65500452024-12-28
00763000311650KYPHON® Bone Filler Device (BFD)F04B2020-11-06
20643169842735KYPHON ELEMENT™ Balloon Kyphoplasty System7480703T2023-06-03
00613994946393n/aEX08108162022-11-21
00643169100725Medtronic Reusable InstrumentsCDS3A2022-10-15
00643169100749Medtronic Reusable InstrumentsCDS2A2022-10-15
00643169100756KYPHON® Cement Delivery SystemCC02A2022-10-15
00763000590970Kyphon VuE Bone Cement and Kyphon MixerCT01B2022-07-25

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