FDA UDI In Commercial Distribution 🇺🇸 United States

ZAVATION

DI: 00842166166523 · Model: 670-7550-1 · ZAVATION LLC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ZAVATION
Primary DI
00842166166523
Version / Model
670-7550-1
Company Name
ZAVATION LLC
Labeler DUNS
069472800
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-10
Public Version
1
Public Version Date
2021-09-20
Public Version Status
New
Public Device Record Key
3baab038-2db4-48e4-befc-00787d095329

Device Description

HA+ 7.5mmx50mm screw

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
Radiation Sterilization

Product Codes

Code Name
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation
KWP Appliance, Fixation, Spinal Interlaminal

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00842166166523

Customer Contacts

Phone
601-919-1119

Premarket Submissions

Submission Number Supplement Number
K211113 000