FDA.reportPublic FDA data

EVOS Lumbar Interbody System

Primary DI
00841193122083
Brand
EVOS Lumbar Interbody System
Company
Cutting Edge Spine, LLC
Model
CES-501
Catalog number
CES-501
Device description
Bayonet Rake Curette
Published
2018-08-31
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information

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
K150321000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K150321000EVOS Lumbar Interbody SystemCutting Edge Spine, LLC2015-07-13MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00841193122083PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00841193122083008411931220838411931220830841193122083

GMDN Terms#

Term, Definition table
TermDefinition
Bone file/rasp, manualA hand-held manual surgical instrument with a surface(s) of coarse and/or fine grooves or teeth designed to scrape and smooth the surface of bone during a surgical procedure. The device is typically a one-piece instrument with grooves/teeth along all or part of its working end(s). It is available in a variety of sizes and working end designs, including straight and curved ends and often double-ended with a central handle. It is not dedicated for use at a specific anatomy (e.g., sinus, ear) and it is made of metal [e.g., stainless steel, titanium (Ti)]. This is a reusable device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Length600Millimeter

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Store at room temperature

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(704)243-0892B.Roof@cuttingedgespine.com

Regulatory Flags#

DUNS number
069472647
Device count
1
Lot or batch
true
Serial number
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00841193127996T-FIX™3Dsi Joint Fusion SystemCES-6432026-03-24
00841193127521EVOL®ha-Hyper C Cervical Interbody System6012-0507A6012-0507A2026-03-11
00841193127538EVOL®ha-Hyper C Cervical Interbody System6012-0607A6012-0607A2026-03-11
00841193127545EVOL®ha-Hyper C Cervical Interbody System6012-0707A6012-0707A2026-03-11
00841193127552EVOL®ha-Hyper C Cervical Interbody System6012-0807A6012-0807A2026-03-11
00841193127569EVOL®ha-Hyper C Cervical Interbody System6012-0907A6012-0907A2026-03-11
00841193127576EVOL®ha-Hyper C Cervical Interbody System6012-1007A6012-1007A2026-03-11
00841193127583EVOL®ha-Hyper C Cervical Interbody System6012-1107A6012-1107A2026-03-11
00841193127590EVOL®ha-Hyper C Cervical Interbody System6012-1207A6012-1207A2026-03-11
00841193127606EVOL®ha-Hyper C Cervical Interbody System6013-0512A6013-0512A2026-03-11
00841193127613EVOL®ha-Hyper C Cervical Interbody System6013-0612A6013-0612A2026-03-11
00841193127620EVOL®ha-Hyper C Cervical Interbody System6013-0712A6013-0712A2026-03-11
00841193127637EVOL®ha-Hyper C Cervical Interbody System6013-0812A6013-0712A2026-03-11
00841193127644EVOL®ha-Hyper C Cervical Interbody System6013-0912A6013-0912A2026-03-11
00841193127651EVOL®ha-Hyper C Cervical Interbody System6013-1012A6013-1012A2026-03-11
00841193127668EVOL®ha-Hyper C Cervical Interbody System6013-1112A6013-1112A2026-03-11
00841193127675EVOL®ha-Hyper C Cervical Interbody System6013-1212A6013-1212A2026-03-11
00841193101934EVOS Lumbar Interbody System4014-0164014-0162015-10-30
00841193104836EVOS Lumbar Interbody System4067-0104067-0102015-10-30
00841193105635EVOS Lumbar Interbody System4004-0144004-0142016-01-12

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
08800043912870N/ATDM Co., Ltd.MAX2026-06-02
08800043912887N/ATDM Co., Ltd.MAX2026-06-02
08800043912894N/ATDM Co., Ltd.MAX2026-06-02
08800043912900N/ATDM Co., Ltd.MAX2026-06-02
08800043912917N/ATDM Co., Ltd.MAX2026-06-02
08800043912924N/ATDM Co., Ltd.MAX2026-06-02
08800043912931N/ATDM Co., Ltd.MAX2026-06-02
08800043912948N/ATDM Co., Ltd.MAX2026-06-02
08800043912955N/ATDM Co., Ltd.MAX2026-06-02
08800043912962N/ATDM Co., Ltd.MAX2026-06-02
08800043912979N/ATDM Co., Ltd.MAX2026-06-02
08800043912986N/ATDM Co., Ltd.MAX2026-06-02
08800043912993N/ATDM Co., Ltd.MAX2026-06-02
08800043913006N/ATDM Co., Ltd.MAX2026-06-02
08800043913013N/ATDM Co., Ltd.MAX2026-06-02
08800043913020N/ATDM Co., Ltd.MAX2026-06-02
08800043913037N/ATDM Co., Ltd.MAX2026-06-02
08800043913044N/ATDM Co., Ltd.MAX2026-06-02
08800043913051N/ATDM Co., Ltd.MAX2026-06-02
08800043913068N/ATDM Co., Ltd.MAX2026-06-02
08800043913075N/ATDM Co., Ltd.MAX2026-06-02
08800043964183N/ATDM Co., Ltd.MAX2026-06-02
08800043964190N/ATDM Co., Ltd.MAX2026-06-02
08800043964206N/ATDM Co., Ltd.MAX2026-06-02
08800043964213N/ATDM Co., Ltd.MAX2026-06-02
08800043964220N/ATDM Co., Ltd.MAX2026-06-02
08800043964237N/ATDM Co., Ltd.MAX2026-06-02
08800043964244N/ATDM Co., Ltd.MAX2026-06-02
08800043964251N/ATDM Co., Ltd.MAX2026-06-02
08800043964268N/ATDM Co., Ltd.MAX2026-06-02