FDA.reportPublic FDA data

Arthrex®

Primary DI
00888867523425
Brand
Arthrex®
Company
ARTHREX, INC.
Model
AR-S8735-20-S
Catalog number
AR-S8735-20-S
Device description
Spine Compression Screw, 3.5x20mm
Published
2025-06-06
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HWCScrew, fixation, bone
MRWSYSTEM, FACET SCREW SPINAL DEVICE

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HWCScrew, Fixation, BoneOrthopedic2
MRWSystem, Facet Screw Spinal DeviceUnknownU

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00888867523425PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00888867523425008888675234258888675234250888867523425

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.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)934-4404complaints@arthrex.com

Regulatory Flags#

DUNS number
131747628
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00888867620612Arthrex®AR-3650DK-1AR-3650DK-12026-10-01
00888867620629Arthrex®AR-3650DK-2AR-3650DK-22026-10-01
00888867620636Arthrex®AR-3650DK-3AR-3650DK-32026-10-01
00888867620643Arthrex®AR-3650DK-4AR-3650DK-42026-10-01
00888867526174Arthrex®AR-S6203-SAR-S6203-S2026-09-29
00888867544291Arthrex®AR-S7500-FAR-S7500-F2026-09-29
00888867618961Arthrex®AR-S1000-C7AR-S1000-C72026-09-28
00888867621237Arthrex®AR-S1000-C7-1AR-S1000-C7-12026-09-28
00888867543904Arthrex®AR-1101TH-13CT-SAR-1101TH-13CT-S2026-09-25
00888867543911Arthrex®AR-1101TH-8CT-SAR-1101TH-8CT-S2026-09-25
00888867543928Arthrex®AR-1101TH-13OT-SAR-1101TH-13OT-S2026-09-25
00888867543935Arthrex®AR-1101TH-8OT-SAR-1101TH-8OT-S2026-09-25
00888867460973Arthrex®AR-9001A-7140CSAR-9001A-7140CS2026-06-11
00888867291690Arthrex®AR-3350-4031AR-3350-40312018-12-13
00888867291751Arthrex®AR-3355-4031AR-3355-40312018-12-13
00888867161085Arthrex®AR-3350-4071AR-3350-40712018-12-13
00888867161207Arthrex®AR-3355-4071AR-3355-40712018-12-13
00888867504059Arthrex®AR-9650CAR-9650C2026-09-21
00888867504066Arthrex®AR-9650C-01AR-9650C-012026-09-21
00888867504073Arthrex®AR-9650C-02AR-9650C-022026-09-21

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
03700569633943NANEWCLIP TECHNICSHWC2026-10-01
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03700569634025NANEWCLIP TECHNICSHWC2026-10-01
03700569634049NANEWCLIP TECHNICSHWC2026-10-01
03700569634063NANEWCLIP TECHNICSHWC2026-10-01
00852776006614CORUS PCSS 3D LevelOne, 4mmProvidence Medical Technology, Inc.MRW2026-09-30
00852776006621CORUS PCSS 3D Implant, 4mmProvidence Medical Technology, Inc.MRW2026-09-30
00852776006706CORUS PCSS 3D Implant, 5mmProvidence Medical Technology, Inc.MRW2026-09-30
08057717550535BRM TOOL Titanium ScrewBRM EXTREMITIES SRLHWC2026-09-30
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08057717550788BRM TOOL Titanium ScrewBRM EXTREMITIES SRLHWC2026-09-30
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