FDA.reportPublic FDA data

NA

Primary DI
04042409049460
Brand
NA
Company
aap Implantate AG
Model
NK 2025-31
Catalog number
NK 2025-31
Device description
K-wire with 2 trocar points, ø2.5, L 310
Published
2016-08-18
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
HTYPIN, FIXATION, SMOOTH

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HTYPin, Fixation, SmoothOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K131459000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K131459000AAP K-WIRE, STEINMANN PIN, CERCLAGE WIREAap Implantate AG2013-10-17JDW

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04042409049460PrimaryGS10
04042409391491Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04042409049460040424090494604042409049460
04042409391491040424093914914042409391491

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
328420633
Device count
10
DM 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
04042409035807NAIP 0104-002018-02-28
04042409035845NAIP 0104-012018-02-28
04042409002939NAIP 8403-002018-02-28
04042409036170NAIP 2505-002018-02-28
04042409207273NAIP 8405-002018-02-28
04042409228995NAIP 8405-502018-02-28
04042409363337NAIP 2506-002018-02-28
04042409387555LOQTEQ®IU 8166-042018-02-28
04042409202711LOQTEQ®PG 3555-04-2PG 3555-04-22016-08-18
04042409202728LOQTEQ®PG 3555-05-2PG 3555-05-22016-08-18
04042409202735LOQTEQ®PG 3555-06-2PG 3555-06-22016-08-18
04042409202742LOQTEQ®PG 3555-07-2PG 3555-07-22016-08-18
04042409202766LOQTEQ®PG 3555-08-2PG 3555-08-22016-08-18
04042409202773LOQTEQ®PG 3555-09-2PG 3555-09-22016-08-18
04042409202797LOQTEQ®PG 3555-10-2PG 3555-10-22016-08-18
04042409202803LOQTEQ®PG 3555-11-2PG 3555-11-22016-08-18
04042409202810LOQTEQ®PG 3555-12-2PG 3555-12-22016-08-18
04042409202827LOQTEQ®PG 3555-14-2PG 3555-14-22016-08-18
04042409202834LOQTEQ®PG 3555-16-2PG 3555-16-22016-08-18
04042409202841LOQTEQ®PG 3555-18-2PG 3555-18-22016-08-18

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Primary DI, Brand, Company table
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07649990202389Handle SSurgical Fusion Technologies GmbHHTY2025-10-01
07649990202396Geomax Reamer SetSurgical Fusion Technologies GmbHHTY2025-10-01
07630037863977APTUSMedartis AGHTY2025-07-31
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07649990202297Guide S-PI / W5.0Surgical Fusion Technologies GmbHHTY2024-04-12
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07649990202327Drill S-PI-A2.3Surgical Fusion Technologies GmbHHTY2024-04-12
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07649990202365Tray SF Push-in Anchor PortfolioSurgical Fusion Technologies GmbHHTY2024-04-12
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