FDA UDI In Commercial Distribution 🇺🇸 United States

Blade® Anterior Cervical Plate System

DI: 00889929000236 · Model: 30-2-36 · NEXXT SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Blade® Anterior Cervical Plate System
Primary DI
00889929000236
Version / Model
30-2-36
Company Name
NEXXT SPINE, LLC
Labeler DUNS
003489810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-29
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
1e39d25c-97aa-4fef-af91-99aed7946470

Device Description

Cervical Plate, 2 Level 36mm

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
No
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00889929000236

Customer Contacts

Phone
317-436-7801

Premarket Submissions

Submission Number Supplement Number
K091936 000

Device Sizes

Type Value Unit Text
Length 36 Millimeter
Device Size Text, specify 2 Level