FDA.reportPublic FDA data

MaxMoreSpine

Primary DI
04260200312624
Brand
MaxMoreSpine
Company
Hoogland Spine Products GmbH
Model
1001-GW 003N
Device description
Nitinol Guide Wire 1,0 mm, 20
Published
2022-03-01
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information

Product Codes#

Code, Name table
CodeName
FZXGuide, Surgical, Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FZXGuide, Surgical, InstrumentGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04260200312624PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04260200312624042602003126244260200312624

GMDN Terms#

Term, Definition table
TermDefinition
Bone nail guidewire, reusableA long, thin, metal rod designed to guide intramedullary canal devices for performing the implantation of an intramedullary nail to treat damaged bone. The rod is usually manually inserted into the canal to typically guide a surgical instrument (e.g., a reamer) and the implantable nail. This device is made of metal [e.g., high-grade stainless steel, titanium (Ti)] and is available in a variety of sizes, lengths, and designs (e.g., round-tip, trocar-tip, or flexible-tip). It may be used in femoral, tibial, humeral or supracondylar intramedullary canals. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
507292204
Device count
1
Premarket exempt
true
Lot or batch
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04260200310774MaxMoreSpine1001-GW 0012022-03-01
04260200310781MaxMoreSpine1001-GW 0022022-03-01
04260200310798MaxMoreSpine1001-GW 0032022-03-01
04260200313010MaxMoreSpine1001-GW 0062022-03-01
04260200313539MaxMoreSpine1001-GW 0082022-03-01
04260200310064MaxMoreSpine1001-AI 0032022-02-28
04260200310323MaxMoreSpine1001-CW 0012022-02-28
04260200314031MaxMoreSpine1001-BD 003C2022-03-15
04260200310187MaxMoreSpine1001-BD 0062022-03-01
04260200310194MaxMoreSpine1001-BD 0072022-03-01
04260200311061MaxMoreSpine1001-TR 0022022-03-01
04260200311078MaxMoreSpine1001-TS 0012022-03-01
04260200311085MaxMoreSpine1001-TS 0022022-03-01
04260200311092MaxMoreSpine1001-TS 0032022-03-01
04260200311542MaxMoreSpine1001-TS 004-12022-03-01
04260200312570MaxMoreSpine1001-CT 002A2022-03-01
04260200312594MaxMoreSpine1001-DR 0012022-03-01
04260200312600MaxMoreSpine1001-DR 0022022-03-01
04260200313034MaxMoreSpine1001-MDT-0012022-03-01
04260200313072MaxMoreSpine1001-TS 0052022-03-01

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00190446960362DYNANAIL HELIXMedshape, Inc.FZX2026-10-09
00190446960379DYNANAIL HELIXMedshape, Inc.FZX2026-10-09
10840143919350AtriClip® Selection GuideATRICURE, INC.FZX2026-10-09
06932503563857Additional Working ChannelMicro-Tech (Nanjing) Co., Ltd.FZX2026-09-30
06932503563864Additional Working ChannelMicro-Tech (Nanjing) Co., Ltd.FZX2026-09-30
06932503563871Additional Working ChannelMicro-Tech (Nanjing) Co., Ltd.FZX2026-09-30
00810056993139corraCarlsmed, Inc.FZX2026-01-30
00810112590036MOTOBAND CPCROSSROADS EXTREMITY SYSTEMSFZX2023-12-05
00810112590043MOTOBAND CPCROSSROADS EXTREMITY SYSTEMSFZX2023-12-05
00810112590050MOTOBAND CPCROSSROADS EXTREMITY SYSTEMSFZX2023-12-05
00810112590067MOTOBAND CPCROSSROADS EXTREMITY SYSTEMSFZX2023-12-05
00810112590098MOTOBAND CPCROSSROADS EXTREMITY SYSTEMSFZX2023-12-05
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