FDA UDI In Commercial Distribution 🇺🇸 United States

Palladian™

DI: 00841508102991 · Model: 50-90-0032 · NEUROSTRUCTURES, INC
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Palladian™
Primary DI
00841508102991
Version / Model
50-90-0032
Company Name
NEUROSTRUCTURES, INC
Labeler DUNS
079391677
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-16
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
91d4dc15-c715-466a-9047-e9c37c175a01

Device Description

Cross Connector Torque Handle

Device Characteristics

Single Use
No
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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
KWP Appliance, Fixation, Spinal Interlaminal
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00841508102991

Customer Contacts

Phone
8003526103