FDA UDI In Commercial Distribution 🇺🇸 United States

Monaco Pedicle Screw System

DI: 00843210125152 · Model: 931-6060 · Altus Spine, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Monaco Pedicle Screw System
Primary DI
00843210125152
Version / Model
931-6060
Company Name
Altus Spine, LLC
Labeler DUNS
078331322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-02
Public Version
1
Public Version Date
2018-11-02
Public Version Status
New
Public Device Record Key
0c0e65e0-a5fc-4b70-aa42-6e9bca80d55a

Device Description

External Hex Pre-Lordosed Rod, Monaco

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
NKB Thoracolumbosacral pedicle screw system
KWQ Appliance, fixation, spinal intervertebral body

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00843210125152

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K181339 000

Device Sizes

Type Value Unit Text
Outer Diameter 6 Millimeter
Length 60 Millimeter