FDA UDI In Commercial Distribution 🇺🇸 United States

Nerve Root Retractor

DI: 10840199500236 · Model: 7233-54 · KOROS U.S.A., INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Nerve Root Retractor
Primary DI
10840199500236
Version / Model
7233-54
Catalog Number
7233-54
Company Name
KOROS U.S.A., INC.
Labeler DUNS
007928633
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-01-31
Public Version
1
Public Version Date
2022-02-08
Public Version Status
New
Public Device Record Key
9315640d-e568-4236-94b9-656125220310

Device Description

Nerve Root Retractor

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
No
PM Exempt
No
Has Serial Number
Yes
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

GMDN Terms

Code Name
42848 External spinal fixation system

Identifiers

Type ID
Primary 10840199500236
Direct Marking 00840199500239

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K875290 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 6.5mm tip 18cm length

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in dry place at room temperature