FDA UDI In Commercial Distribution 🇺🇸 United States

NEO Modera Pedicle Screw System

DI: 00815730020187 · Model: A · NEW ERA ORTHOPEDICS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NEO Modera Pedicle Screw System
Primary DI
00815730020187
Version / Model
A
Catalog Number
3RST55-140
Company Name
NEW ERA ORTHOPEDICS LLC
Labeler DUNS
079375910
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-20
Public Version
5
Public Version Date
2020-05-14
Public Version Status
Update
Public Device Record Key
f13a38d0-b9ff-4d20-bde3-b3134b876ab5

Device Description

Rod, Straight, Titanium, Ø5.5mm x 140mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
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
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

Code Name
37272 Trans-facet-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00815730020187

Customer Contacts

Phone
7175856785

Premarket Submissions

Submission Number Supplement Number
K141253 000