FDA.reportPublic FDA data

GoPLF! Posterior Lateral Fusion Device

Primary DI
07640387660133
Brand
GoPLF! Posterior Lateral Fusion Device
Company
GetSet Surgical SA
Model
3207555
Device description
GoPLF! Posterior Lateral Fusion Device, 2 Screws, Multi-Axial Titanium Screw, 7.5 x 55mm
Published
2023-12-12
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
NKBThoracolumbosacral Pedicle Screw System

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NKBThoracolumbosacral Pedicle Screw SystemOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07640387660133PrimaryGS10
07640387660546Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07640387660133076403876601337640387660133
07640387660546076403876605467640387660546

GMDN Terms#

Term, Definition table
TermDefinition
Spinal bone screw, non-bioabsorbableA small, threaded, implantable rod with a screw head and drive intended 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 (e.g., surgical steel, titanium alloy, carbon fibre). It is available in various types (e.g., pedicle or transfacet, with a slotted, cross, star, or polygonal drive), and is typically used to provide immobilization and stabilization of spinal segments in the treatment of spinal instabilities or deformities. A screw head adaptor intended to stabilize a rod may be included with the screw.

Regulatory Flags#

DUNS number
480143831
Device count
2
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07640387660140GoPLF! Posterior Lateral Fusion Device31000102023-12-12
07640387660003GoPLF! Posterior Lateral Fusion Device32055352022-02-21
07640387660010GoPLF! Posterior Lateral Fusion Device32055402022-02-21
07640387660027GoPLF! Posterior Lateral Fusion Device32055452022-02-21
07640387660034GoPLF! Posterior Lateral Fusion Device32055502022-02-21
07640387660041GoPLF! Posterior Lateral Fusion Device32065352022-02-21
07640387660058GoPLF! Posterior Lateral Fusion Device32065402022-02-21
07640387660065GoPLF! Posterior Lateral Fusion Device32065452023-12-12
07640387660072GoPLF! Posterior Lateral Fusion Device32065502023-12-12
07640387660089GoPLF! Posterior Lateral Fusion Device32065552023-12-12
07640387660096GoPLF! Posterior Lateral Fusion Device32075352023-12-12
07640387660102GoPLF! Posterior Lateral Fusion Device32075402023-12-12
07640387660119GoPLF! Posterior Lateral Fusion Device32075452023-12-12
07640387660126GoPLF! Posterior Lateral Fusion Device32075502023-12-12
07640387660157GoPLF! Posterior Lateral Fusion Device32000352023-12-12
07640387660164GoPLF! Posterior Lateral Fusion Device32000402023-12-12
07640387660171GoPLF! Posterior Lateral Fusion Device32000452023-12-12
07640387660188GoPLF! Posterior Lateral Fusion Device32000502023-12-12
07640387660195GoPLF! Posterior Lateral Fusion Device32000552023-12-12
07640387660201GoPLF! Posterior Lateral Fusion Device32000602023-12-12

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
B678520297S0PressON™NEXUS SPINE, L.L.C.NKB2026-07-10
B678520298S0PressON™NEXUS SPINE, L.L.C.NKB2026-07-10
B678520299S0PressONNEXUS SPINE, L.L.C.NKB2026-07-10
B678520300S0PressON™NEXUS SPINE, L.L.C.NKB2026-07-10
B678520301S0PressONNEXUS SPINE, L.L.C.NKB2026-07-10
B678520302S0PressON™NEXUS SPINE, L.L.C.NKB2026-07-10
B678520303S0PressONNEXUS SPINE, L.L.C.NKB2026-07-10
B678520304S0PressON™NEXUS SPINE, L.L.C.NKB2026-07-10
B678520305S0PressONNEXUS SPINE, L.L.C.NKB2026-07-10
B678520306S0PressON™NEXUS SPINE, L.L.C.NKB2026-07-10
B678520485S0PressON Pedicle Screw SystemNEXUS SPINE, L.L.C.NKB2026-07-10
B678520486S0PressON Pedicle Screw SystemNEXUS SPINE, L.L.C.NKB2026-07-10
B678520487S0PressON Pedicle Screw SystemNEXUS SPINE, L.L.C.NKB2026-07-10
B678520488S0PressON Pedicle Screw SystemNEXUS SPINE, L.L.C.NKB2026-07-10
B678520489S0PressON Pedicle Screw SystemNEXUS SPINE, L.L.C.NKB2026-07-10
B678520490S0PressON Pedicle Screw SystemNEXUS SPINE, L.L.C.NKB2026-07-10
B678520491S0PressON Pedicle Screw SystemNEXUS SPINE, L.L.C.NKB2026-07-10
B678520492S0PressON Pedicle Screw SystemNEXUS SPINE, L.L.C.NKB2026-07-10
B678520493S0PressON Pedicle Screw SystemNEXUS SPINE, L.L.C.NKB2026-07-10
B678520494S0PressON Pedicle Screw SystemNEXUS SPINE, L.L.C.NKB2026-07-10
B678520495S0PressON Pedicle Screw SystemNEXUS SPINE, L.L.C.NKB2026-07-10
B678520496S0PressON Pedicle Screw SystemNEXUS SPINE, L.L.C.NKB2026-07-10
00643169465879MSB CD HORIZON Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.NKB2026-06-28
10889981441555VIRATASeaspine Orthopedics CorporationNKB2026-06-24
10889981441609VIRATASeaspine Orthopedics CorporationNKB2026-06-24
10889981441616VIRATASeaspine Orthopedics CorporationNKB2026-06-24
10889981441623VIRATASeaspine Orthopedics CorporationNKB2026-06-24
10889981441661VIRATASeaspine Orthopedics CorporationNKB2026-06-24
10889981065348MarinerSeaspine Orthopedics CorporationNKB2016-09-02
10889981065539MarinerSeaspine Orthopedics CorporationNKB2016-09-02