FDA.reportPublic FDA data

Inertia® Pedicle Screw System

Primary DI
00889929001134
Brand
Inertia® Pedicle Screw System
Company
NEXXT SPINE, LLC
Model
10-10-4555
Device description
Polyaxial Pedicle Screw, Ø4.5mm x 55mm
Published
2015-07-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
KWPAppliance, Fixation, Spinal Interlaminal
MNHOrthosis, Spondylolisthesis Spinal Fixation
MNIOrthosis, Spinal Pedicle Fixation

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWPAppliance, Fixation, Spinal InterlaminalOrthopedic2
MNHOrthosis, Spondylolisthesis Spinal FixationOrthopedic2
MNIOrthosis, Spinal Pedicle FixationOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K101278000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K101278000INERTIA PEDICLE SCREW SYSTEMNexxt Spine, LLC2010-12-20MNH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00889929001134PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00889929001134008899290011348899290011340889929001134

GMDN Terms#

Term, Definition table
TermDefinition
Spinal bone screw, non-bioabsorbableA small, threaded, implantable rod with a slotted head intended to be used for internal spinal fixation by being screwed into the spine to hold a correction/stabilization device (e.g., rod, plate, tether) to bone; it is made of a material that is not chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). The device is available in various types, including pedicle and transfacet, and is typically used to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Length55Millimeter
Outer Diameter4.5Millimeter

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
317-436-7801Support@nexxtspine.com

Regulatory Flags#

DUNS number
003489810
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00840067212189TrellOss®-A SA432H00142026-06-24
00840067212196TrellOss®-A SA432H00192026-06-24
00840067212202TrellOss®-A SA432H00202026-06-24
00840067212219TrellOss®-A SA432H00212026-06-24
00840067212226TrellOss®-A SA432H00222026-06-24
00840067212233TrellOss®-A SA432H00232026-06-24
00840067212240TrellOss®-A SA432H00242026-06-24
00840067212257TrellOss®-A SA432H01082026-06-24
00840067212264TrellOss®-A SA432H01102026-06-24
00840067212271TrellOss®-A SA432H01122026-06-24
00840067212288TrellOss®-A SA432H01142026-06-24
00840067212295TrellOss®-A SA432H01162026-06-24
00840067212301TrellOss®-A SA432H01182026-06-24
00840067212318TrellOss®-A SA432H01202026-06-24
00889929072752NEXXT MATRIXX® Stand Alone ALIF SystemI61-03-022026-06-24
00889929072769NEXXT MATRIXX® Stand Alone ALIF SystemI61-20-072026-06-24
00889929072776NEXXT MATRIXX® Stand Alone ALIF SystemI61-20-082026-06-24
00889929072783NEXXT MATRIXX® Stand Alone ALIF SystemI61-22-062026-06-24
00889929072424Matrixx SystemI92-20-022026-05-27
00889929072523Struxxure® Plate System63-55T-152026-05-14

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00643169465879MSB CD HORIZON Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.MNH2026-06-28
00643169465879MSB CD HORIZON Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.KWP2026-06-28
00643169465879MSB CD HORIZON Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.MNI2026-06-28
00643169101296MSB VERTEX® Reconstruction SystemMEDTRONIC SOFAMOR DANEK, INC.KWP2026-06-27
10889981441555VIRATASeaspine Orthopedics CorporationKWP2026-06-24
10889981441609VIRATASeaspine Orthopedics CorporationKWP2026-06-24
10889981441616VIRATASeaspine Orthopedics CorporationKWP2026-06-24
10889981441623VIRATASeaspine Orthopedics CorporationKWP2026-06-24
10889981441661VIRATASeaspine Orthopedics CorporationKWP2026-06-24
10889981005115NewportSeaspine Orthopedics CorporationMNH2015-09-24
10889981005115NewportSeaspine Orthopedics CorporationMNI2015-09-24
10889981005139NewportSeaspine Orthopedics CorporationMNI2015-09-24
10889981005139NewportSeaspine Orthopedics CorporationMNH2015-09-24
10889981005146NewportSeaspine Orthopedics CorporationMNI2015-09-24
10889981005146NewportSeaspine Orthopedics CorporationMNH2015-09-24
10889981005290NewportSeaspine Orthopedics CorporationMNI2015-09-24
10889981005290NewportSeaspine Orthopedics CorporationMNH2015-09-24
10889981005306NewportSeaspine Orthopedics CorporationMNH2015-09-24
10889981005306NewportSeaspine Orthopedics CorporationMNI2015-09-24
10889981005313NewportSeaspine Orthopedics CorporationMNI2015-09-24
10889981005313NewportSeaspine Orthopedics CorporationMNH2015-09-24
10889981005320NewportSeaspine Orthopedics CorporationMNH2015-09-24
10889981005320NewportSeaspine Orthopedics CorporationMNI2015-09-24
10889981005337NewportSeaspine Orthopedics CorporationMNH2015-09-24
10889981005337NewportSeaspine Orthopedics CorporationMNI2015-09-24
10889981005344NewportSeaspine Orthopedics CorporationMNI2015-09-24
10889981005344NewportSeaspine Orthopedics CorporationMNH2015-09-24
10889981005351NewportSeaspine Orthopedics CorporationMNH2015-09-24
10889981005351NewportSeaspine Orthopedics CorporationMNI2015-09-24
10889981005634NewportSeaspine Orthopedics CorporationMNI2015-09-24