FDA UDI In Commercial Distribution 🇺🇸 United States

Silverstone Interbody Fusion System

DI: B417SP2610121 · Model: SP261012 · Altus Spine, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Silverstone Interbody Fusion System
Primary DI
B417SP2610121
Version / Model
SP261012
Company Name
Altus Spine, LLC
Labeler DUNS
078331322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-28
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
c2e80dbd-e720-45ab-839a-439ffa0fc572

Device Description

26 x 10 x 12 mm, PEEK 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
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary B417SP2610121
Secondary 00843210118536

Customer Contacts

Device Sizes

Type Value Unit Text
Length 26 Millimeter
Angle 7 degree
Height 12 Millimeter
Width 10 Millimeter