FDA UDI In Commercial Distribution 🇺🇸 United States

Zavation

DI: 00842166195141 · Model: 410-9000 · ZAVATION LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zavation
Primary DI
00842166195141
Version / Model
410-9000
Company Name
ZAVATION LLC
Labeler DUNS
069472800
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-21
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
64188d1b-e6bf-44ac-856d-a82fd8cc0232

Device Description

Cortical Screw System Implant Tray

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
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
NKB Thoracolumbosacral Pedicle Screw System
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00842166195141

Customer Contacts

Phone
601-919-1119

Premarket Submissions

Submission Number Supplement Number
K190317 000