FDA UDI In Commercial Distribution 🇺🇸 United States

Silverstone Titanium Interbody Fusion System

DI: B417ST528071 · Model: ST52807 · Altus Spine, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Silverstone Titanium Interbody Fusion System
Primary DI
B417ST528071
Version / Model
ST52807
Company Name
Altus Spine, LLC
Labeler DUNS
078331322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-22
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
6a10e25b-3855-4005-8752-f9a0401d50aa

Device Description

28x10x07mm 5degree PEEK Silverstone-T

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
Yes
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 B417ST528071
Secondary 00843210104133

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K170512 000

Device Sizes

Type Value Unit Text
Length 28 Millimeter
Angle 5 degree
Width 10 Millimeter
Height 7 Millimeter