FDA.reportPublic FDA data

BIOFOAM

Primary DI
00889797014892
Brand
BIOFOAM
Company
WRIGHT MEDICAL TECHNOLOGY, INC.
Model
46002095
Catalog number
46002095
Device description
Wedge Trial
Published
2016-09-17
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HWCScrew, fixation, bone
HWTTEMPLATE

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HWCScrew, Fixation, BoneOrthopedic2
HWTTemplateOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00889797014892PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00889797014892008897970148928897970148920889797014892

GMDN Terms#

Term, Definition table
TermDefinition
Surgical implant template, reusableA device designed to determine the appropriate size and placement of a non-dental implant for a patient prior to or during implantation surgery. It is typically available as a graduated set or an individual plate (e.g., a translucent plastic sheet or a cut metal shape) with patterns/sizes corresponding to the size of the implant to be used to aid the surgeon in final selection of implant size, placement, and/or adaption. It is used for, e.g., total- or partial-joint prostheses, bone fracture fixation implants (plates, nails, including skull plate implants) or other types of surgical implants. This is a reusable device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Height9.5Millimeter
Length20Millimeter

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(800)238-7117customerservice@wmt.com

Regulatory Flags#

DUNS number
807201207
Device count
1
Premarket 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
00889797076586INVISION60004403600044032022-05-31
00840420167606INVISION600044032016-02-26
00840420106254DARCODC0043162015-10-01
00840420106261DARCODC0043182015-10-01
00840420106278DARCODC0043202015-10-01
00840420106285DARCODC0043222015-10-01
00840420106292DARCODC0043242015-10-01
00889797023443INVISION600025012016-09-17
00889797024136INVISION600124002016-09-17
00889797024143INVISION600124012016-09-17
00889797040686NA49411XL2016-09-17
00889797040693NA49412XL2016-09-17
00889797040709NA49413XL2016-09-17
00889797057295EZ FRAMEEF0037002015-10-24
00889797058452EZ FRAME SIDEKICKEF0016002016-09-17
00889797102957NAEF002550EF0025502022-06-23
00889797103084NAEF003005EF0030052022-06-23
00889797103107NAEF003700EF0037002022-06-23
00889797103091NAEF003010EF0030102022-06-23
00889797103046NAEF001600EF0016002022-05-31

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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07613154320486MATTAStryker GmbHHWC2023-10-20
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07613154320523MATTAStryker GmbHHWC2023-10-20
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07613154320592MATTAStryker GmbHHWC2023-10-20
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07613154320646MATTAStryker GmbHHWC2023-10-20
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07613154320691MATTAStryker GmbHHWC2023-10-20
07613154320769MATTAStryker GmbHHWC2023-10-20
07613154320776MATTAStryker GmbHHWC2023-10-20
07613154320820MATTAStryker GmbHHWC2023-10-20
07613154320837MATTAStryker GmbHHWC2023-10-20
07613154320844MATTAStryker GmbHHWC2023-10-20
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07613154320875MATTAStryker GmbHHWC2023-10-20
07613154320899MATTAStryker GmbHHWC2023-10-20
07613154320912MATTAStryker GmbHHWC2023-10-20