ZAVATION NANOPRIME LABYRINTH LLIF

Primary DI
00197157080860
Brand
ZAVATION NANOPRIME LABYRINTH LLIF
Company
Zavation LLC
Model
NLL2545-0012
Device description
NANOPRIME LABYRINTH LLIF 25MM X 45MM, 0°, 12MM
Published
2026-05-07
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

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

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWPAppliance, Fixation, Spinal InterlaminalOrthopedic2
OVDIntervertebral Fusion Device With Integrated Fixation, LumbarOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K233509000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K233509000Zavation IBF System, Zavation Varisync Plate System and Varisync Spacer System, LABYRINTH System, Zavation ALIF SystemZavation Medical Products, LLC2024-04-10MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00197157080860PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00197157080860001971570808601971570808600197157080860

GMDN Terms#

Term, Definition table
TermDefinition
Spinal fixation plate, non-bioabsorbableA small, implantable, non-customized sheet of solid material intended to be attached to the spine with screws for spinal immobilization as part of treatment of a spinal instability or deformity; it is made of a material that is not chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). Disposable instruments intended to facilitate implantation, or fixation implants (i.e., bone screws), may be packaged with the plate.

Sterilization Methods#

Method table
Method
Radiation Sterilization

Contacts#

Phone, Email table
PhoneEmail
6019191119info@zavation.com

Regulatory Flags#

DUNS number
069472800
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00197157113384ZAVATION SCREW1011-O-045085-S-S2026-09-04
00197157113391ZAVATION SCREW1011-O-045090-S-S2026-09-04
00197157113407ZAVATION SCREW1011-O-045095-S-S2026-09-04
00197157113414ZAVATION SCREW1011-O-045100-S-S2026-09-04
00197157113421ZAVATION SCREW1011-O-045105-S-S2026-09-04
00197157113438ZAVATION SCREW1011-O-045110-S-S2026-09-04
00197157113445ZAVATION SCREW1011-O-045025-C-C2026-09-04
00197157113452ZAVATION SCREW1011-O-045030-C-C2026-09-04
00197157113469ZAVATION SCREW1011-O-045035-C-C2026-09-04
00197157113476ZAVATION SCREW1011-O-045040-C-C2026-09-04
00197157113483ZAVATION SCREW1011-O-045045-C-C2026-09-04
00197157113490ZAVATION SCREW1011-O-045050-C-C2026-09-04
00197157113506ZAVATION SCREW1011-O-045055-C-C2026-09-04
00197157113513ZAVATION SCREW1011-O-045060-C-C2026-09-04
00197157113520ZAVATION SCREW1011-O-045065-C-C2026-09-04
00197157113537ZAVATION SCREW1011-O-045070-C-C2026-09-04
00197157113544ZAVATION SCREW1011-O-045075-C-C2026-09-04
00197157113551ZAVATION SCREW1011-O-045080-C-C2026-09-04
00197157113568ZAVATION SCREW1011-O-045085-C-C2026-09-04
00197157113575ZAVATION SCREW1011-O-045090-C-C2026-09-04

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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10888857002098DENALI® MI Spinal SystemVB Spine LLCKWP2015-09-24