FDA UDI In Commercial Distribution 🇺🇸 United States

Yellowstone

DI: B587P11092670 · Model: 1 · SUMMIT SPINE LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Yellowstone
Primary DI
B587P11092670
Version / Model
1
Catalog Number
P110926-7
Company Name
SUMMIT SPINE LLC
Labeler DUNS
079539689
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-27
Public Version
2
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
016fafb5-1baf-4493-a5c2-e209cb208a3a

Device Description

11mm PLIF Implant 9mm Wide 26mm Length, 7 deg Lordosis

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary B587P11092670

Customer Contacts

Phone
8772089272

Device Sizes

Type Value Unit Text
Width 9 Millimeter
Length 26 Millimeter
Height 11 Millimeter
Angle 7 degree