FDA.reportPublic FDA data

n/a

Primary DI
00643169402423
Brand
n/a
Company
MEDTRONIC SOFAMOR DANEK, INC.
Model
9010000515
Device description
GUIDE PIN 9010000515 2MM TROCAR
Published
2025-10-16
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
GDFGUIDE, NEEDLE, SURGICAL

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GDFGuide, Needle, SurgicalGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00643169402423PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00643169402423006431694024236431694024230643169402423

GMDN Terms#

Term, Definition table
TermDefinition
Spinal guidewireA thin, non-implantable rod intended to guide the insertion of a cannulated orthopaedic implant (typically a screw) and/or surgical instrument (e.g., cannula, drill bit) during spinal surgery. This is a single-use device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(800)633-8766Corporate.UDI@medtronic.com

Regulatory Flags#

DUNS number
830350380
Device count
1
Premarket exempt
true
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00199150081073Medtronic Reusable InstrumentsX04260042026-07-30
20763000211015Medtronic Reusable Instrument65501022022-10-16
20763000211039Medtronic Reusable Instrument65502022022-10-16
00763000311667KYPHON® Directional Bone Filler DeviceF04C2020-11-06
00763000311681KYPHON® EXPRESS™ Bone Filler DeviceF06A2020-11-06
00763000311698KYPHON® EXPRESS™ Directional Bone Filler DeviceF06B2020-11-06
0076300031183413 Ga TampVPT02A2020-11-06
00763000883478N/a7480757T2025-06-01
00763000883485N/a7480758T2025-06-01
00763000711993N/A65500422024-12-28
00763000712006N/A65500432024-12-28
00763000712013N/A65500442024-12-28
00763000712020n/a65500452024-12-28
00763000311650KYPHON® Bone Filler Device (BFD)F04B2020-11-06
20643169842735KYPHON ELEMENT™ Balloon Kyphoplasty System7480703T2023-06-03
00613994946393n/aEX08108162022-11-21
00643169100725Medtronic Reusable InstrumentsCDS3A2022-10-15
00643169100749Medtronic Reusable InstrumentsCDS2A2022-10-15
00643169100756KYPHON® Cement Delivery SystemCC02A2022-10-15
00763000590970Kyphon VuE Bone Cement and Kyphon MixerCT01B2022-07-25

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00850084501012Xpansion® Micro-Autografting KitNEW HORIZON HEALTHCARE MANAGEMENT LLCGDF2026-07-28
06976712970334Hemo NeedleMicro-Energy Medical Technology Co., LtdGDF2026-07-13
04048223069738TunnEler 235Pajunk GmbH MedizintechnologieGDF2026-06-10
10197344044795MEDLINEMEDLINE INDUSTRIES, INC.GDF2025-09-23
10197344044801MEDLINEMEDLINE INDUSTRIES, INC.GDF2025-09-23
ESAM14762481STOMA®Storz am Mark GmbHGDF2025-04-30
07630037864523APTUSMedartis AGGDF2025-04-08
07630037864547APTUSMedartis AGGDF2025-04-08
07630037864561APTUSMedartis AGGDF2025-04-08
07630037864585APTUSMedartis AGGDF2025-04-08
08056138586338MarkXM.D.L. S.R.L.GDF2025-02-28
08057276004715MarkXM.D.L. S.R.L.GDF2025-02-28
10197106342312CARDINAL HEALTHCardinal Health 200, LLCGDF2024-04-01
07630037864165APTUSMedartis AGGDF2024-03-22
ESAM14755481STOMA®Storz am Mark GmbHGDF2023-11-20
ESAM14760481STOMA®Storz am Mark GmbHGDF2023-06-05
ESAM14761481STOMA®Storz am Mark GmbHGDF2023-06-05
ESAM14750481STOMA®Storz am Mark GmbHGDF2022-11-07
ESAM14751481STOMA®Storz am Mark GmbHGDF2022-11-07
08033860028596BIOPSYBELLBIOPSYBELL SRLGDF2022-09-16
08033860028602BIOPSYBELLBIOPSYBELL SRLGDF2022-09-16
08033860030353BIOPSYBELLBIOPSYBELL SRLGDF2022-09-16
10840199505767Needle HolderKOROS U.S.A., INC.GDF2022-04-01
10840199505774Needle HolderKOROS U.S.A., INC.GDF2022-04-01
10840199505798Needle HolderKOROS U.S.A., INC.GDF2022-04-01
10840199505804Needle HolderKOROS U.S.A., INC.GDF2022-04-01
10840199505811Needle HolderKOROS U.S.A., INC.GDF2022-04-01
10840199505828Needle HolderKOROS U.S.A., INC.GDF2022-04-01
10840199505835Needle HolderKOROS U.S.A., INC.GDF2022-04-01
10840199505842Needle HolderKOROS U.S.A., INC.GDF2022-04-01