FDA.reportPublic FDA data

Tiger

Primary DI
00812926023960
Brand
Tiger
Company
Trilliant Surgical, LLC
Model
210-60-006
Device description
0.062in x 6in K-Wire Double Ended
Published
2017-03-15
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
HTYPin, Fixation, Smooth
LXHOrthopedic Manual Surgical Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HTYPin, Fixation, SmoothOrthopedic2
LXHOrthopedic Manual Surgical InstrumentOrthopedic1

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K121008000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K121008000TRILLIANT SURGICAL K-WIRESTrilliant Surgical, Ltd.2012-06-04HTY

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00812926023960PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00812926023960008129260239608129260239600812926023960

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
Device Size Text, specify0

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
828829072
Device count
1
DM exempt
true
Premarket exempt
true
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00190446898801Arsenal Foot330-60-0062026-03-19
00810028397385Tiger201-30-0422024-06-04
00810028399099Tiger201-40-2102024-06-04
00810028399464Tiger203-20-0162024-06-04
00850062461949Tibial Impactor Tips 920-0061-042024-08-09
00810028391840Arsenal Ankle340-00-0032022-05-02
00812926028804Hook Tamp320-00-0202019-03-11
008129260201293S Hemi111-00-0022018-09-23
008129260202283S Hemi111-00-0122018-09-23
00812926027043Two-Step Hammertoe214-00-0142018-09-23
008129260280333S Hemi111-00-0132018-09-23
00812926028187Staple Tamp510-00-0052018-09-23
00810028398344Tiger201-20-0082024-05-31
00810028395343Arsenal Foot300-82-0252024-03-27
00810028395206Arsenal Foot300-82-0112024-03-21
00810028395213Arsenal Foot300-82-0122024-03-21
00810028395220Arsenal Foot300-82-0132024-03-21
00810028395237Arsenal Foot300-82-0142024-03-21
00810028395244Arsenal Foot300-82-0152024-03-21
00810028395251Arsenal Foot300-82-0162024-03-21

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G4533312BT0PEAK MEDICALPeak Medical Distribution Inc.LXH2026-06-03
07613327648355PANGEAStryker GmbHLXH2026-06-02
07613327648379PANGEAStryker GmbHLXH2026-06-02
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