Ventana A

Primary DI
00840606187626
Brand
Ventana A
Company
SPINAL ELEMENTS, INC.
Model
40060-030
Device description
Ø6.0MM BONE SCREW, 30MM LONG
Published
2026-10-22
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
OVDIntervertebral fusion device with integrated fixation, lumbar

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
OVDIntervertebral Fusion Device With Integrated Fixation, LumbarOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840606187626PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840606187626008406061876268406061876260840606187626

GMDN Terms#

Term, Definition table
TermDefinition
Metal-polymer composite spinal interbody fusion cageA device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is typically in the form of a hollow, porous, threaded and/or fenestrated device made of a non-bioabsorbable synthetic polymer with a metallic coating that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be packaged with the cage.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(760)607-0121info@spinalelements.com

Regulatory Flags#

DUNS number
610712213
Device count
1
DM exempt
true
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
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
00840466901011Primus66027-0452026-10-22
00840606168472SAPPHIRE X27002-0232026-10-22
00840606168502SAPPHIRE X27002-0292026-10-22
00840606174855Primus66102-0002026-10-22
00840606175142Primus66647-0002026-10-22
00840606175203Primus66656-0002026-10-22
00840606175234Primus66685-0002026-10-22
00840606176347Lucent11341-1122026-10-22
00840606184656Overwatch108-159-01C2026-10-22
00840606184847Lucent11341-5122026-10-22
00840606185820Primus66599-0002026-10-22
00840606185868Primus66675-0102026-10-22
00840606186506Lateral81077-0082026-10-22
00840606186513Lateral81077-0102026-10-22
00840606186575SAPPHIRE X27001-0002026-10-22
00840606186612SAPPHIRE X27001-000-042026-10-22
00840606186643SAPPHIRE X27001-000-072026-10-22
00840606186674SAPPHIRE X27001-000-102026-10-22
00840606186704SAPPHIRE X27001-000-132026-10-22
00840606186735SAPPHIRE X27001-000-162026-10-22

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Primary DI, Brand, Company table
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