FDA.reportPublic FDA data

3DP Lumbar Interbody System

Primary DI
M719GLL102M12150
Brand
3DP Lumbar Interbody System
Company
Genesys Orthopedics Systems LLC
Model
1
Catalog number
GLL102-M1215
Device description
LLIF Ingot Trial, Medium 12mm x 15-Degree
Published
2024-04-12
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MQPSpinal Vertebral Body Replacement Device
ODPIntervertebral Fusion Device With Bone Graft, Cervical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2
MQPSpinal Vertebral Body Replacement DeviceOrthopedic2
ODPIntervertebral Fusion Device With Bone Graft, CervicalOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
M719GLL102M12150PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic cement restrictor sizerA non-sterile, hand-held manual orthopaedic surgical instrument designed to be used to measure the diameter of the medullary canal of a bone (e.g., femur, humerus) in order to select the appropriate size orthopaedic cement restrictor implant. It may be in the form of a trial prosthesis attached to an inserter, or a rod with a measuring gauge at the distal end. This is a reusable device intended to be sterilized prior to use.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Angle6degree
Length20Millimeter

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
512-381-7070info@genesysspine.com

Regulatory Flags#

DUNS number
017921066
Device count
1
DM exempt
true
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
M719GLL11403DP Lumbar Interbody System1GLL1142026-10-19
M719GLL11503DP Lumbar Interbody System1GLL1152026-10-19
M719GLL11603DP Lumbar Interbody System1GLL1162026-10-19
M719GSIX1270Sacroiliac Joint Fusion System1GSI-X1272026-10-19
M719GSIX1210TiLock1GSI-X1212026-08-18
M719IST80030C0TiLock1IS-T80030-C2026-08-18
M719IST80035C0TiLock1IS-T80035-C2026-08-18
M719IST80040C0TiLock1IS-T80040-C2026-08-18
M719IST80045C0TiLock1IS-T80045-C2026-08-18
M719IST80050C0TiLock1IS-T80050-C2026-08-18
M719IST80055C0TiLock1IS-T80055-C2026-08-18
M719IST80060C0TiLock1IS-T80060-C2026-08-18
M719IST80065C0TiLock1IS-T80065-C2026-08-18
M719IST80070C0TiLock1IS-T80070-C2026-08-18
M719IST80075C0TiLock1IS-T80075-C2026-08-18
M719IST80080C0TiLock1IS-T80080-C2026-08-18
M719IST80085C0TiLock1IS-T80085-C2026-08-18
M719IST80090C0TiLock1IS-T80090-C2026-08-18
M719IST80095C0TiLock1IS-T80095-C2026-08-18
M719IST80100C0TiLock1IS-T80100-C2026-08-18

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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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
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08809974809624Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
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08809974809648Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
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08809974837856Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
08809974837955Anyplus II Spinal Fixation SystemGS Medical Co., Ltd.MAX2025-12-19
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