FDA.reportPublic FDA data

Brickyard Stand-Alone ALIF

Primary DI
00843210179780
Brand
Brickyard Stand-Alone ALIF
Company
Altus Spine, LLC
Model
1030-0000
Device description
Implant Inserter
Published
2024-08-30
Public version status
New
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
MAXIntervertebral fusion device with bone graft, lumbar

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00843210179780PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00843210179780008432101797808432101797800843210179780

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic implant inserter/extractor, reusableA hand-held manual surgical instrument designed to insert or extract an implantable orthopaedic device (e.g., a bone nail, spiral blade, or bone fixation plate) through application of a striking or screwing force. It is an instrument in a one-piece or modular configuration with a mechanism that will attach and/or lock to part of the implant, and a mechanism to apply the striking force (e.g., on a pad/flange) using a surgical hammer or a weight that can slide along a shaft, or a mechanism for twisting (screwing) (e.g., T-handle). This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(610)355-4156Info@altus-spine.com

Regulatory Flags#

DUNS number
078331322
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
true
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
00843210189505Brickyard Stand-Alone ALIF1030-0101G-452025-09-02
00843210190457Brickyard Stand-Alone ALIF1030-3215G-452025-09-02
00843210190464Brickyard Stand-Alone ALIF1030-3220G-452025-09-02
00843210190471Brickyard Stand-Alone ALIF1030-3225G-452025-09-02
00843210190488Brickyard Stand-Alone ALIF1030-3230G-452025-09-02
00843210190495Brickyard Stand-Alone ALIF1030-3235G-452025-09-02
00843210190501Brickyard Stand-Alone ALIF1030-3240G-452025-09-02
00843210176567Sochi300-09012025-03-13
00843210170749Indy Standalone1030-0301G-452024-10-07
00843210189154Brickyard Stand-Alone ALIF1020-20002024-10-07
00843210189437Brickyard Stand-Alone ALIF1030-0301G-452024-10-07
00843210159492Indy StandaloneSL382716122024-10-04
00843210161358Indy StandaloneSL38271612T2024-10-04
00843210169118Indy Standalone1030-42152024-10-04
00843210169125Indy Standalone1030-42202024-10-04
00843210169132Indy Standalone1030-42252024-10-04
00843210169149Indy Standalone1030-42302024-10-04
00843210169156Indy Standalone1030-42352024-10-04
00843210169163Indy Standalone1030-42402024-10-04
00843210169170Indy Standalone1030-02152024-10-04

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Primary DI, Brand, Company table
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