FDA UDI In Commercial Distribution 🇺🇸 United States

NIAGARA® Lateral Access System

DI: 10888857519954 · Model: PRO-1021-04 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NIAGARA® Lateral Access System
Primary DI
10888857519954
Version / Model
PRO-1021-04
Catalog Number
PRO-1021-04
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-11
Public Version
2
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
24fa20e2-2b23-4149-8ffd-f284ff2d1436

Device Description

Straight Blade, Size 20x80 mm

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
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 10888857519954

Customer Contacts

Device Sizes

Type Value Unit Text
Width 20 Millimeter
Length 80 Millimeter