ShurFit Lumbar Interbody

Primary DI
00840019952255
Brand
ShurFit Lumbar Interbody
Company
PRECISION SPINE, INC.
Model
72-OPC-3616
Catalog number
72-OPC-3616
Device description
36 x 16mm 12° Oblique PEEK Interbody
Published
2023-03-16
Public version status
New
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

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K212075000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K212075000ShurFit Lumbar Interbody SystemPrecision Spine, Inc.2021-12-08MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840019952255PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840019952255008400199522558400199522550840019952255

GMDN Terms#

Term, Definition table
TermDefinition
Extra-gynaecological surgical mesh, silk, non-bioabsorbableA non-bioabsorbable, implantable material (e.g., flat sheet) made from silk (derived from domesticated silkworms) intended for extra-gynaecological, non-dental tissue repair/reinforcement application(s) [e.g., pericardial reinforcement, plastic surgery, abdominal hernia repair]. Disposable devices associated with implantation may be supplied with the mesh.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
079398589
Device count
1
Lot or batch
true
Manufacturing date on label
true
Sterilization required before use
true

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