FDA.reportPublic FDA data

K wire 250mm

Primary DI
09348215075811
Brand
K wire 250mm
Company
SIGNATURE ORTHOPAEDICS PTY LTD
Model
191-07-1013
Device description
The saleable unit (device count) is 1, there are 5 K wires in the saleable unit
Published
2020-09-09
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
LXHOrthopedic Manual Surgical Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LXHOrthopedic Manual Surgical InstrumentOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
09348215075811PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
09348215075811093482150758119348215075811

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.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
751993028
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
09348215039295Liner Impactor112-152-0022018-10-09
09348215039301Liner Impactor112-152-3342018-10-09
09348215039318Liner Impactor112-152-1212018-10-09
09348215039325Liner Impactor112-152-0032018-10-09
09348215039332Ceramic Liner Inserter Impactor Head112-152-2102018-10-09
09348215039349Ceramic Liner Inserter Impactor Head112-152-2112018-10-09
09348215039356Ceramic Liner Inserter Impactor Head112-152-2122018-10-09
09348215039363Ceramic Liner Inserter Impactor Head112-152-2132018-10-09
09348215039387Ceramic Liner Impact Adaptor112-152-3052018-10-09
09348215039615Quick Release Head Impactor112-212-0172018-10-09
09348215039837Quick Release Stem Impactor112-212-0062018-10-09
09348215040758Head Impactor112-28-00112018-10-09
09348215040796Stem Impactor112-28-00292018-10-09
09348215040826Monoblock Head Impactor112-28-00382018-10-09
09348215040888Mjolnir112-28-00602018-10-12
09348215041250Femoral Impactor122-15-04642018-10-09
09348215041779Tibial Impactor122-15-04622018-10-09
09348215137427Swivel Stem Impactor112-32-03132025-10-10
09348215137434Swivel Stem Impactor - Long112-32-0314 2025-10-10
09348215152673Proximal Reamer Ø12111-552-4222025-09-16

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