Align

Primary DI
00810043486682
Brand
Align
Company
ACUITY SURGICAL DEVICES, LLC
Model
16-22551512
Device description
Align Ti Lateral Interbody 22x55x15 12°
Published
2024-01-12
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
OVDIntervertebral Fusion Device With Integrated Fixation, LumbarOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K221535000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K221535000Align Lumbar Interbody Fusion SystemAcuity Surgical Devices, LLC2022-07-22MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810043486682PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810043486682008100434866828100434866820810043486682

GMDN Terms#

Term, Definition table
TermDefinition
Metallic 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 metal [e.g., titanium (Ti)] 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.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Angle12degree
Height15Millimeter
Length22Millimeter
Width55Millimeter

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
8442284890support@acuitysurgical.com

Regulatory Flags#

DUNS number
025855111
Device count
1
DM exempt
true
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810192476657Tera20-1000007220-100000722026-02-10
00810192476664Tera20-1000007120-100000712026-02-10
00810192476671Tera20-1000007320-100000732026-02-10
00810043485043Align11-102550-SP2023-01-11
00810043485050Align11-140003-SP2023-01-11
00810043485210Align11-102050-SP2023-01-11
00810043485227Align11-102055-SP2023-01-11
00810043485234Align11-102555-SP2023-01-11
00810043485241Align11-103050-SP2023-01-11
00810043485258Align11-103055-SP2023-01-11
00810161113101Stabilis35-141205002024-07-11
00810161113118Stabilis35-141205052024-07-11
00810161113125Stabilis35-141206002024-07-11
00810161113132Stabilis35-141206052024-07-11
00810161113149Stabilis35-141206102024-07-11
00810161113156Stabilis35-141207002024-07-11
00810161113163Stabilis35-141207052024-07-11
00810161113170Stabilis35-141207102024-07-11
00810161113187Stabilis35-141207152024-07-11
00810161113194Stabilis35-141208002024-07-11

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00197157074197ZAVATION SCREWZavation LLCOVD2026-05-29
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00197157074227ZAVATION SCREWZavation LLCOVD2026-05-29
00197157074234ZAVATION SCREWZavation LLCOVD2026-05-29
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