FDA.reportPublic FDA data

MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK

Primary DI
00841732136366
Brand
MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK
Company
CTL Medical Corporation
Model
013.2306
Device description
MATISSE™ ACIF Cage, Titanium-PEEK - W20 x L16, 8Deg., H6mm
Published
2023-10-05
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
ODPIntervertebral Fusion Device With Bone Graft, Cervical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
ODPIntervertebral Fusion Device With Bone Graft, CervicalOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K121569000
K172212000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K121569000MATISSE ANTERIOR CERVICAL INTERBODY FUSION CAGE SYSTEMAccel Spine2012-07-27ODP
K172212000MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK™Ctl Medical Corporation2018-01-09ODP

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00841732136366PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00841732136366008417321363668417321363660841732136366

GMDN Terms#

Term, Definition table
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 table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(214)545-5820schedule@ctlamedica.com

Regulatory Flags#

DUNS number
080138504
Device count
1
Lot or batch
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00841732155671VALEO II PL OL Interbody Fusion System12.301.10122023-09-27
00841732155688VALEO II PL OL Interbody Fusion System12.301.10132023-09-27
00841732155695VALEO II PL OL Interbody Fusion System12.301.10152023-09-27
00841732155701VALEO II PL OL Interbody Fusion System12.301.10142023-09-27
00841732155718VALEO II PL OL Interbody Fusion System12.301.10162023-09-27
00841732155725VALEO II PL OL Interbody Fusion System12.301.15082023-09-27
00841732155732VALEO II PL OL Interbody Fusion System12.301.15092023-09-27
00841732155749VALEO II PL OL Interbody Fusion System12.301.15102023-09-27
00841732155756VALEO II PL OL Interbody Fusion System12.301.15112023-09-27
00841732155763VALEO II PL OL Interbody Fusion System12.301.15122023-09-27
00841732155770VALEO II PL OL Interbody Fusion System12.301.15132023-09-27
00841732155787VALEO II PL OL Interbody Fusion System12.301.15142023-09-27
00841732155794VALEO II PL OL Interbody Fusion System12.301.15152023-09-27
00841732155800VALEO II PL OL Interbody Fusion System12.301.15162023-09-27
00841732156135VALEO II PL OL Interbody Fusion System12.301.20072023-09-27
00841732156142VALEO II PL OL Interbody Fusion System12.301.20082023-09-27
00841732156159VALEO II PL OL Interbody Fusion System12.301.20092023-09-27
00841732156166VALEO II PL OL Interbody Fusion System12.301.20102023-09-27
00841732156173VALEO II PL OL Interbody Fusion System12.301.20112023-09-27
00841732156180VALEO II PL OL Interbody Fusion System12.301.20122023-09-27

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00810017913664Saber-C Body (PT), 12x15x7 6 deg.ELEVATION SPINE, INC.ODP2026-06-05
00810017914609Saber-C Plate, 14x17x6 12 deg.ELEVATION SPINE, INC.ODP2026-06-05
00810017914616Saber-C Plate, 14x17x7 12 deg.ELEVATION SPINE, INC.ODP2026-06-05
00810017914623Saber-C Plate, 14x17x8 12 deg.ELEVATION SPINE, INC.ODP2026-06-05
00810017915354Saber-C, Spike Driver 5-7, MedialELEVATION SPINE, INC.ODP2026-06-05
00810017915361Saber-C, Spike Driver 5-7, LateralELEVATION SPINE, INC.ODP2026-06-05
00810017915378Saber-C, Spike Driver 8-9, MedialELEVATION SPINE, INC.ODP2026-06-05
00810017915385Saber-C, Spike Driver 8-9, LateralELEVATION SPINE, INC.ODP2026-06-05
08809986491008BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-04
08809986491015BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-04
08809986491022BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-04
08809986491039BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-04
08809986491046BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-04
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08809986491060BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-04
08809986491077BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-04
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08809986491121BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-04
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08809986490766BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-03
08809986490773BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-03
08809986490780BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-03
08809986490797BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-03
08809986490803BluEX Cervical Expandable Cage SystemL&K BIOMED CO. ,LTD.ODP2026-06-03
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