FDA UDI In Commercial Distribution 🇺🇸 United States

Yellowstone

DI: B528XL0624700 · Model: 1 · PANTHEON SPINAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Yellowstone
Primary DI
B528XL0624700
Version / Model
1
Catalog Number
XL062470
Company Name
PANTHEON SPINAL, LLC
Labeler DUNS
071012634
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-18
Public Version
1
Public Version Date
2021-07-26
Public Version Status
New
Public Device Record Key
f1cef652-c175-4c85-b2f7-2afd52813906

Device Description

Lateral Implant 6mm H x 24mm W x 70mm L - Parallel

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 B528XL0624700

Customer Contacts

Phone
5123083488

Premarket Submissions

Submission Number Supplement Number
K170572 000

Device Sizes

Type Value Unit Text
Height 6 Millimeter
Length 70 Millimeter
Width 24 Millimeter