Copperhead

Primary DI
B014C4110
Brand
Copperhead
Company
EMINENT SPINE LLC
Model
C4110
Published
2017-02-08
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MQPSpinal Vertebral Body Replacement Device
ODPIntervertebral Fusion Device With Bone Graft, Cervical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2
MQPSpinal Vertebral Body Replacement DeviceOrthopedic2
ODPIntervertebral Fusion Device With Bone Graft, CervicalOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K090064000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K090064000EMINENT SPINE INTERBODY FUSION SYSTEMEminent Spine2009-04-09MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B014C4110PrimaryHIBCC0

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

Regulatory Flags#

DUNS number
022576742
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
B014DB100DiamondbackDB1002017-02-08
B014DB1030DiamondbackDB10302017-02-08
B014DB1035DiamondbackDB10352017-02-08
B014DB1040DiamondbackDB10402017-02-08
B014DB1045DiamondbackDB10452017-02-08
B014DB1050DiamondbackDB10502017-02-08
B014DB1055DiamondbackDB10552017-02-08
B014DB1060DiamondbackDB10602017-02-08
B014DB1065DiamondbackDB10652017-02-08
B014DB1070DiamondbackDB10702017-02-08
B014DB1075DiamondbackDB10752017-02-08
B014DB1080DiamondbackDB10802017-02-08
B014DB1085DiamondbackDB10852017-02-08
B014DB1090DiamondbackDB10902017-02-08
B014DB1095DiamondbackDB10952017-02-08
B014DB1100DiamondbackDB11002017-02-08
B014DB1110DiamondbackDB11102017-02-08
B014DB1120DiamondbackDB11202017-02-08
B014DB1130DiamondbackDB11302017-02-08
B014DB1140DiamondbackDB11402017-02-08

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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