FDA.reportPublic FDA data

restor3d Lumbar Implant

Primary DI
00840097508023
Brand
restor3d Lumbar Implant
Company
Restor3d, Inc.
Model
1113-M1215
Device description
Lumbar ALIF Implant, Medium Footprint, 28x35, 12 mm Height, 15°
Published
2023-10-30
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K220523000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K220523000restor3d TiDAL Lumbar Interbody Fusion DeviceRestor3D2022-06-17MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840097508023PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840097508023008400975080238400975080230840097508023

GMDN Terms#

Term, Definition table
TermDefinition
Interspinous spinal fixation implantAn implantable device intended to be attached to two adjacent vertebral spinous processes to provide immobilization and stabilization of spinal segments as an adjunct to bony fusion in the treatment of spinal conditions (e.g., degenerative disc disease, spondylolisthesis, tumour, trauma). It is intended to be used on the thoracic, lumbar or sacral spine during a minimally-invasive procedure. It is made of metal [e.g., titanium (Ti), nickel-titanium alloy (Nitinol)] and may incorporate bone graft pockets. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
080819836
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00840097503677Veritas Instrumentation6500-11202026-10-16
00840097536705Identity CR KA5253-0001TCR-000- D0012026-09-25
00840097536712Identity CR KA5253-0002TCR-000- D0012026-09-25
00840097536729Identity CR KA 3DP Porous5253-0031TCR-000-D0052026-09-25
00840097536736Identity CR KA 3DP Porous5253-0032TCR-000-D0052026-09-25
00840097536743Identity CR KA 3DP Porous5253-0021TCR-000-SPEC2026-09-25
00840097536750Identity CR KA 3DP Porous5253-0011TCR-000-SPEC2026-09-25
00840097536767Identity CR KA 3DP Porous5253-0022TCR-000-SPEC2026-09-25
00840097536774Identity CR KA 3DP Porous5253-0012TCR-000-SPEC2026-09-25
00840097536781Identity CR KA5253-0901TCR-000-D0012026-09-25
00840097536798Identity CR KA5253-0902TCR-000-D0012026-09-25
00840097536804Identity CR KA 3DP Porous5253-0933TCR-000-D0052026-09-25
00840097536811Identity CR KA 3DP Porous5253-0934TCR-000-D0052026-09-25
00840097533919Veritas Hemiarthroplasty1508-10012026-09-18
00840097533926Veritas Hemiarthroplasty1510-38142026-09-18
00840097533933Veritas Hemiarthroplasty1510-40152026-09-18
00840097533940Veritas Hemiarthroplasty1510-42162026-09-18
00840097533957Veritas Hemiarthroplasty1510-44172026-09-18
00840097533964Veritas Hemiarthroplasty1510-46182026-09-18
00840097533971Veritas Hemiarthroplasty1510-48182026-09-18

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
08809974809440Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809457Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809464Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809471Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809488Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809495Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809501Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809518Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809525Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809532Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809549Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809556Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809563Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809570Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809587Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809594Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809600Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809617Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809624Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809631Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809648Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809655Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974809662Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974818879Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974836231Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974836286Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974837856Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974837955Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974839355Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974849590Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19