FDA.reportPublic FDA data

2mm Pre-Bent Wedge VL Gridlock Plate

Primary DI
00812926022604
Brand
2mm Pre-Bent Wedge VL Gridlock Plate
Company
Trilliant Surgical, LLC
Model
300-54-102
Published
2017-02-28
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Single use
true

Product Codes#

Code, Name table
CodeName
HRSPlate, Fixation, Bone

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HRSPlate, Fixation, BoneOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K130964000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K130964000GRIDLOCK PLATING SYSTEMTrilliant Surgical, Ltd.2013-05-08HRS

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00812926022604PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00812926022604008129260226048129260226040812926022604

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic fixation plate, non-bioabsorbable, non-sterileA non-sterile implantable sheet of firm material intended to be attached to fractured long bone fragments with screws to bridge and stabilize the fracture gap, and shield the site from stress as the bone heals; the material is not chemically degraded or absorbed by natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). The device is typically used to treat traumatic or pathological orthopaedic fractures; it may also be used to temporarily augment bone following a lengthening procedure, or for arthrodesis (joint fusion). This device is intended to be sterilized prior to use.

Device Sizes#

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

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

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

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810028393431STAR PSI Tibia Cut Guide601-01-0002022-11-30
00810028393448STAR PSI Tibia Anatomical Model601-01-0012022-11-30
00810028393455STAR PSI Talus Cut Guide601-02-0002022-11-30
00810028393462STAR PSI Talus Anatomical Model601-02-0012022-11-30
00810028394971STAR PSI Standard Bundle with Anatomical Models601-00-0012022-11-30
0081292602720310mm Evans Plate300-54-2102017-03-15
0081292602721012mm Evans Plate300-54-2122017-03-15
00812926027791Tissue Retractor317-00-0072018-09-23
00812926027869Subtalar Implant System Sterilization Tray Lid112-99-0112018-09-23
0081292602851410 Hole Gridlock Helical Plate, Right300-65-0042018-10-15
00812926027036Tiger210-00-1022018-09-23
00812926027890Tiger210-99-1122018-09-23
00812926028002Gridlock320-99-1132018-09-23
00812926028026Gridlock310-00-0212018-09-23
00190446972020Generic Instrument215-00-0072026-07-16
00190446972037Generic Instrument215-00-0082026-07-16
00190446900498Arsenal Foot330-60-0072026-06-25
00190446900504Arsenal Foot330-60-0082026-06-25
00190446917861Arsenal Foot330-01-2152026-06-25
00190446917878Arsenal Foot330-01-2162026-06-25

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Primary DI, Brand, Company table
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08809986482549CastleLoc Pectus Bar SystemL&K BIOMED CO. ,LTD.HRS2026-09-22
08809986482556CastleLoc Pectus Bar SystemL&K BIOMED CO. ,LTD.HRS2026-09-22
08809986482563CastleLoc Pectus Bar SystemL&K BIOMED CO. ,LTD.HRS2026-09-22
08809986482570CastleLoc Pectus Bar SystemL&K BIOMED CO. ,LTD.HRS2026-09-22
08809986482587CastleLoc Pectus Bar SystemL&K BIOMED CO. ,LTD.HRS2026-09-22
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03700569602949Alians ForearmNEWCLIP TECHNICSHRS2024-11-14
03700569602956Alians ForearmNEWCLIP TECHNICSHRS2024-11-14
03700569602963Alians ForearmNEWCLIP TECHNICSHRS2024-11-14
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03700569602987Alians ForearmNEWCLIP TECHNICSHRS2024-11-14
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