ALEUTIAN® Interbody Systems

Primary DI
10888857488656
Brand
ALEUTIAN® Interbody Systems
Company
VB Spine LLC
Model
SP-4164-01
Catalog number
SP-4164-01
Device description
Parallel Trial, Size 22x50x6 mm
Published
2020-08-17
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
MAXIntervertebral fusion device with bone graft, lumbar

Product Code Classifications#

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

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K150481000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K150481000Cascadia Interbody SystemK2m, Inc.2015-08-20MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10888857488656PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
1088885748865610888857488656

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic prosthesis implantation instrument, reusableA hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments. It may be used for the following applications: 1) to hold/align/fix bone preparation instruments, prosthesis, or prosthesis component; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface between prosthesis components. This is a reusable device intended to be sterilized prior to use.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Height6Millimeter
Length50Millimeter
Width22Millimeter

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(703)777-3155mark.zellers@stryker.com

Regulatory Flags#

DUNS number
119508156
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10888857578951Q Interbody Instruments8020-900168020-900162026-03-03
10888857579866Q Interbody Instruments8020-900158020-900152026-03-03
10888857579880Q Interbody Instruments8020-900148020-900142026-03-03
10888857599710YUKON OCT Spinal SystemPRO-1435PRO-14352026-08-25
10888857556072CASCADIA Interbody System8030-900328030-900322024-01-04
10888857557260CASCADIA Interbody System8030-900008030-900002024-01-04
10888857557277CASCADIA Interbody System8030-900018030-900012024-01-04
10888857383746CASCADIA™ Interbody System7902-900387902-900382021-01-29
10888857383753CASCADIA™ Interbody System7902-900397902-900392021-01-29
10888857383814CASCADIA™ Interbody System7902-900457902-900452021-01-29
10888857313354VIKOS® Allograft System2504-900592504-900592020-01-08
10888857326408VIKOS® Allograft System2504-900572504-900572020-01-08
10888857596740NAPA Access System8030-100228030-100222026-07-31
10888857596757NAPA Access System8030-100238030-100232026-07-31
10888857596764NAPA Access System8030-100248030-100242026-07-31
10888857596771NAPA Access System8030-100258030-100252026-07-31
10888857596788NAPA Access System8030-100268030-100262026-07-31
10888857596795NAPA Access System8030-100278030-100272026-07-31
10888857596801NAPA Access System8030-100288030-100282026-07-31
10888857596818NAPA Access System8030-100298030-100292026-07-31

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Primary DI, Brand, Company table
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