FDA UDI In Commercial Distribution 🇺🇸 United States

Tritanium TL

DI: 07613327369366 · Model: 48932086 · Stryker Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tritanium TL
Primary DI
07613327369366
Version / Model
48932086
Catalog Number
48932086
Company Name
Stryker Corporation
Labeler DUNS
149183167
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-28
Public Version
2
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
63482f19-eb62-41de-90d5-51753d9369f9

Device Description

Curved Posterior Lumbar Cage

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 07613327369366

Device Sizes

Type Value Unit Text
Height 8.0 Millimeter
Width 10.0 Millimeter
Angle 6.0 degree
Length 31.0 Millimeter