FDA UDI In Commercial Distribution 🇺🇸 United States

Silverstone Titanium Interbody Fusion System

DI: B417SP301009T1 · Model: SP301009T · 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
B417SP301009T1
Version / Model
SP301009T
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
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
303b316a-3df0-4e27-8aec-c8e252a1279e

Device Description

30L PLIF Titanium Silverstone-P

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
57805 Metallic spinal fusion cage, non-sterile

Identifiers

Type ID
Primary B417SP301009T1
Secondary 00843210106526

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K170512 000

Device Sizes

Type Value Unit Text
Length 30 Millimeter
Angle 7 degree
Width 10 Millimeter
Height 9 Millimeter