FDA UDI In Commercial Distribution 🇺🇸 United States

Zavation

DI: 00842166150058 · Model: 470-162260-00 · ZAVATION LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zavation
Primary DI
00842166150058
Version / Model
470-162260-00
Company Name
ZAVATION LLC
Labeler DUNS
069472800
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-12
Public Version
4
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
b5cbe895-731e-4e04-8699-6d08507f2a10

Device Description

16x22x60mm, 0°, MILC

Device Characteristics

Single Use
Yes
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 00842166150058

Customer Contacts

Phone
601-919-1119

Premarket Submissions

Submission Number Supplement Number
K112700 000
K143228 000