FDA.report

Imola-Silverstone

Primary DI
00843210133461
Brand
Imola-Silverstone
Company
Altus Spine, LLC
Model
600-3107
Device description
Targeting Instrument
Published
2018-10-06
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
false

Related Records

Contact Domains

Product Codes

CodeName
MAXIntervertebral fusion device with bone graft, lumbar

Product Code Classifications

CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00843210133461PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00843210133461008432101334618432101334610843210133461

GMDN Terms

TermDefinition
Polymeric spinal interbody fusion cageA device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Contacts

PhoneEmail
+1(610)355-4156Info@altus-spine.com

Regulatory Flags

DUNS number
078331322
Device count
1
DM exempt
false
Premarket exempt
true
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

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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
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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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