FDA.reportPublic FDA data

NA

Primary DI
H6792926560
Brand
NA
Company
Synthes GmbH
Model
292.656
Catalog number
292656
Device description
2.0MM NON-THREADED GUIDE WIRE- SPADE POINT ON ONE END 230MM
Published
2015-09-14
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
LRNWire, surgical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LRNWire, SurgicalOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10886982180797PrimaryGS10
H6792926560SecondaryHIBCC0

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
1088698218079710886982180797

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

Contacts#

Phone, Email table
PhoneEmail
+1(800)255-2500xx@xx.xx

Regulatory Flags#

DUNS number
486711679
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10705034712307NA03.604.002036040022016-12-31
10705034712802NA03.606.011036060112016-12-31
10705034714592NA03.613.012036130122016-12-31
10705034767819VentroFix304.8343048342016-12-31
10705034768939NA314.0643140642016-12-31
10705034768960Click'X314.0673140672016-12-31
10705034768977Click'X314.0683140682016-12-31
10705034768984Click'X314.0693140692016-12-31
10705034769646NA328.0263280262016-12-31
10705034772608NA388.3643883642016-12-31
10705034775401NA389.2883892882016-12-31
10705034777375NA394.5853945852016-12-31
20705034764051NA292.0202920202019-08-29
00863176000317FIBULINKFGS-1100FGS11002020-03-26
00863176000324FIBULINKFGS-1300FGS13002020-03-26
00863176000300FIBULINKFGS-1000FGS10002017-06-08
10886982113078NA04.130.260S04130260S2016-03-15
10886982077868NA03.311.010033110102015-09-14
10886982077875NA03.311.011033110112015-09-14
10886982077882NA03.311.012033110122015-09-14

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00840124516496FibFixFUSION ORTHOPEDICS, LLCLRN2026-04-09
00840124516502FibFixFUSION ORTHOPEDICS, LLCLRN2026-04-09
00840124517509FibFixFUSION ORTHOPEDICS, LLCLRN2026-04-09
00840124517516FibFixFUSION ORTHOPEDICS, LLCLRN2026-04-09
00840124518551FibFixFUSION ORTHOPEDICS, LLCLRN2026-04-09
00840124524712FuzeFix Max FTFUSION ORTHOPEDICS, LLCLRN2025-11-03
00840124521599FuzeFix Max FTFUSION ORTHOPEDICS, LLCLRN2025-09-17
00840124521674FuzeFix Max FTFUSION ORTHOPEDICS, LLCLRN2025-09-17
00840124514843FuzeRightFUSION ORTHOPEDICS, LLCLRN2025-01-07
00840124514782LapiLockFUSION ORTHOPEDICS, LLCLRN2025-01-06
00840124514799LapiLockFUSION ORTHOPEDICS, LLCLRN2025-01-06
00840124514805LapiLockFUSION ORTHOPEDICS, LLCLRN2025-01-06
00840124514812LapiLockFUSION ORTHOPEDICS, LLCLRN2025-01-06
00840124514829LapiLockFUSION ORTHOPEDICS, LLCLRN2025-01-06
00840124514836LapiLockFUSION ORTHOPEDICS, LLCLRN2025-01-06
00673978047690ATLAS® Cable SystemMEDTRONIC SOFAMOR DANEK, INC.LRN2021-12-19
M20922794K-Wire with stop 1.0mmBIOPRO, INC.LRN2020-08-05
20705034764051NASynthes GmbHLRN2019-08-29
H9812920200NASYNTHES (U.S.A.) LPLRN2019-08-29
10603295210320NADEPUY INTERNATIONAL LTDLRN2018-09-24
00889024035546NAZimmer, Inc.LRN2017-09-26
M209206660K-Wire with stop 1.0mmBIOPRO, INC.LRN2017-08-13
10603295067740CONTROLDEPUY ORTHOPAEDICS, INC.LRN2017-07-21
20673978047885ATLAS® Cable SystemMEDTRONIC SOFAMOR DANEK, INC.LRN2016-06-25
20673978047977ATLAS® Cable SystemMEDTRONIC SOFAMOR DANEK, INC.LRN2016-06-25
20673978048004ATLAS® Cable SystemMEDTRONIC SOFAMOR DANEK, INC.LRN2016-06-25
04546540568083Dall-MilesHowmedica Osteonics Corp.LRN2015-09-24
04546540568090Dall-MilesHowmedica Osteonics Corp.LRN2015-09-24
04546540568106Dall-MilesHowmedica Osteonics Corp.LRN2015-09-24
04546540568113Dall-MilesHowmedica Osteonics Corp.LRN2015-09-24