FDA.reportPublic FDA data

N/A

Primary DI
00889024022362
Brand
N/A
Company
Zimmer, Inc.
Model
262-13
Published
2015-09-24
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
JDWPIN, FIXATION, THREADED

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
JDWPin, Fixation, ThreadedOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00889024022362PrimaryGS10
00889024409811Unit of UseGS10
70889024022361Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00889024022362008890240223628890240223620889024022362
00889024409811008890244098118890244098110889024409811
7088902402236170889024022361

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic bone wireA wire intended for the fixation of bone fractures that may be implanted or used short-term (e.g., to hold a plate in the correct position during an intervention). It may be used: 1) as a cerclage wire to aid bone fixation; 2) in a loop or figure-of-eight configuration to reattach, e.g., the tip of the elbow (olecranon), tibial tubercle, or greater trochanter; 3) to augment bone screw/plate fixation; or 4) as a Kirschner wire or K-Wire to stiffen (arthrodese) a toe or finger. It is made of metal [e.g., stainless steel, cobalt-chrome (Co-Cr)], and may be malleable or rigid; some types include a nut designed to be attached to the wire to prevent wire migration. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0
Length9Inch

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(800)348-2759zimmer.consumerrelations@zimmer.com
+1(800)348-2759zimmer.consumerrelations@zimmerbiomet.com

Regulatory Flags#

DUNS number
056038268
Device count
6
DM exempt
false
Premarket exempt
false
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
00887868150876Affixus®8151113008151113002026-03-20
00887868150333Affixus®8151103008151103002026-03-19
00887868150340Affixus®8151103208151103202026-03-19
00887868150357Affixus®8151103408151103402026-03-19
00887868150364Affixus®8151103608151103602026-03-19
00887868150371Affixus®8151103808151103802026-03-19
00887868150388Affixus®8151104008151104002026-03-19
00887868150395Affixus®8151104208151104202026-03-19
00887868150401Affixus®8151114208151114202026-03-19
00887868150555Affixus®8151123008151123002026-03-19
00887868150562Affixus®8151123208151123202026-03-19
00887868150579Affixus®8151123408151123402026-03-19
00887868150586Affixus®8151123608151123602026-03-19
00887868150593Affixus®8151123808151123802026-03-19
00887868150609Affixus®8151124008151124002026-03-19
00887868150616Affixus®8151124208151124202026-03-19
00887868150883Affixus®8151113208151113202026-03-19
00887868150890Affixus®8151113408151113402026-03-19
00887868150906Affixus®8151113608151113602026-03-19
00887868150913Affixus®8151113808151113802026-03-19

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
08032909626380ST.A.R. 90 F4CITIEFFE SRLJDW2026-03-17
00888867516441Arthrex®ARTHREX, INC.JDW2026-03-13
08051739535730ST.A.R. 90 F4CITIEFFE SRLJDW2026-03-10
00810184540007Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540014Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540021Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540038Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540045Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540052Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540069Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540076Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540083Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540090Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540304Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540311Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540328Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540335Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540342Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540359Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540366Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540373Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540380Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
00810184540397Meduloc Intramedullary Fracture Fixation (IFF) SystemMEDULOC, LLCJDW2026-01-14
14053613294574Tech Knee PackGebr. Brasseler GmbH & Co. KGJDW2026-01-06
08033201841716ILIZAROV SYSTEMSMEDICALPLASTIC SRLJDW2025-08-20
08033201841723ILIZAROV SYSTEMSMEDICALPLASTIC SRLJDW2025-08-20
08033201841754ILIZAROV SYSTEMSMEDICALPLASTIC SRLJDW2025-08-20
08033201841761ILIZAROV SYSTEMSMEDICALPLASTIC SRLJDW2025-08-20
08059386747391DOLPHIXCITIEFFE SRLJDW2025-04-02
24053613293116Navigation PinGebr. Brasseler GmbH & Co. KGJDW2025-03-28