FDA.reportPublic FDA data

restor3d Lumbar Instrumentation

Primary DI
00840097509716
Brand
restor3d Lumbar Instrumentation
Company
Restor3d, Inc.
Model
5113-B7002
Device description
Large Cobb Straight 28mm
Published
2024-04-17
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
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
K234087000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K234087000restor3d TIDAL Lumbar Interbody Fusion SystemRestor3D2024-01-22MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840097509716PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840097509716008400975097168400975097160840097509716

GMDN Terms#

Term, Definition table
TermDefinition
General internal orthopaedic fixation system implantation kitA collection of instruments and devices intended to be used for the placement of an internal orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It is a non-dedicated device that includes various metallic and/or plastic reusable devices [e.g., retractors, rods, clamps, drills, pins, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of internal orthopaedic fixation system; the implant(s) is not included. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
080819836
Device count
1
Lot or batch
true
Donation ID number
true
Sterilization required before use
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
00810017916191SABER-XA, Expandable Spacer, 37x28mm, 16mm, (18°)ELEVATION SPINE, INC.MAX2026-10-27
08809974869284Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809885799977Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809885799984Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809885799991Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974779934Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974779941Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974779958Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974779965Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974779972Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974779989Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974779996Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974789957Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974789964Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974789971Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974789988Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974789995Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799864Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799871Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799888Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799895Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799901Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799918Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799925Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799932Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799949Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799956Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799963Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799970Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18
08809974799987Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-18