OMEGA XP

Primary DI
00840606186551
Brand
OMEGA XP
Company
SPINAL ELEMENTS, INC.
Model
11412-295
Device description
OMEGA XP INSERTER INNER SHAFT
Published
2026-09-22
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
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
KWPAppliance, Fixation, Spinal Interlaminal

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWPAppliance, Fixation, Spinal InterlaminalOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840606186551PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840606186551008406061865518406061865510840606186551

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic prosthesis implantation positioning instrument, reusableA hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments [e.g., drill sleeves and guide wires (Kirschner wires), patella saw guide]. It may be used for the following applications: 1) to hold/align/fix/guide other instruments, prostheses, or prosthesis components; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface (non-adaptive) between prosthesis components. This is a reusable device intended to be sterilized prior to use.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
7606070121customerservice@spinalelements.com

Regulatory Flags#

DUNS number
610712213
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
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
00840606185929Primus66585-0032026-09-24
00840606185936Primus66586-0122026-09-24
00840606186773Primus66586-0142026-09-24
00840606186780Primus66586-0162026-09-24
00840606187237Primus66900-0202026-09-24
00840606187244Primus66900-020-012026-09-24
00840606187251Primus66900-020-022026-09-24
00840606174923Primus66545-0552026-09-22
00840606175036Primus66585-0002026-09-22
00840606175074Primus66515-0002026-09-22
00840606175098Primus66595-0002026-09-22
00840606175135Primus66650-0002026-09-22
00840606175241Primus66690-0002026-09-22
00840606185875Primus66675-0022026-09-22
00840606185899Primus66657-0002026-09-22
00840606186544OMEGA XP11422-0022026-09-22
00840606186797Primus66585-0042026-09-22
00840606190695Primus66910-0002026-09-22
00840606190701Primus66910-000-012026-09-22
00840606190718Primus66910-000-022026-09-22

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00885074494722TSRH® Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.KWP2015-08-05
00613994568311TSRH® Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.KWP2015-08-05
00613994568823TSRH® Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.KWP2015-08-05
00613994888143TSRH® Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.KWP2015-08-05
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