FDA.reportPublic FDA data

TFN-ADVANCE

Primary DI
H679040384100
Brand
TFN-ADVANCE
Company
Synthes GmbH
Model
04.038.410
Catalog number
04038410
Device description
TFNA FENESTRATED HELICAL BLADE 110MM
Published
2017-10-07
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
HSBROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HSBRod, Fixation, Intramedullary And AccessoriesOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K160167000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K160167000DePuy Synthes TFNA Augmentation SystemSynthes (USA) Products, LLC2016-09-26HSB

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10886982099327PrimaryGS10
H679040384100SecondaryHIBCC0

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
1088698209932710886982099327

GMDN Terms#

Term, Definition table
TermDefinition
Spiral bladeAn implantable, rod-like, cannulated device with spiralled flutes at the distal end and a smooth cylindrical portion at the proximal end that is used in combination with a bone fixation plate or an intramedullary nail to support bone fragments after fractures, particularly in the proximal femur or proximal humerus (the bone heads). It is made of metal that cannot be chemically degraded (e.g., surgical steel, titanium alloy). It is intended to decrease the amount of removed bone required for device insertion, and provides a support surface in the zone requiring support (bone head) and resistance to bending in the zone most subject to torque.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(800)255-2500xx@xx.xx

Regulatory Flags#

DUNS number
486711679
Device count
1
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
10705034764030NA291.991.01S29199101S2015-09-14
10705034764047NA291.992.01S29199201S2015-09-14
10705034769097NA321.1313211312016-12-31
10705034769134NA321.7453217452016-12-31
10705034784786NA491.991.01S49199101S2015-09-14
10705034784793NA491.992.01S49199201S2015-09-14
10886982198167NA391.1083911082016-12-31
10886982198204NA391.2013912012016-12-31
10887587078540NASD03.501.442SD035014422026-07-29
10886982362179NASD03.043.006SD030430062026-07-24
10887587078557NASD03.503.067SD035030672026-07-24
10887587078564NASD03.503.072SD035030722026-07-24
10705034712307NA03.604.002036040022016-12-31
10705034712802NA03.606.011036060112016-12-31
10705034714592NA03.613.012036130122016-12-31
10705034767819VentroFix304.8343048342016-12-31
10705034768939NA314.0643140642016-12-31
10705034768960Click'X314.0673140672016-12-31
10705034768977Click'X314.0683140682016-12-31
10705034768984Click'X314.0693140692016-12-31

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Primary DI, Brand, Company table
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