FDA UDI In Commercial Distribution 🇺🇸 United States

VERTEFIX

DI: 06009708426147 · Model: CZ7535CT · ELITE SURGICAL SUPPLIES (PTY) LTD
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VERTEFIX
Primary DI
06009708426147
Version / Model
CZ7535CT
Catalog Number
CZ7535CT
Company Name
ELITE SURGICAL SUPPLIES (PTY) LTD
Labeler DUNS
568359710
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-24
Public Version
1
Public Version Date
2020-02-03
Public Version Status
New
Public Device Record Key
2fd83771-ff4a-483e-be03-42dfc69f3316

Device Description

MULTI AXIAL PEDICLE SCREW 7.5 X 35

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation
KWP Appliance, Fixation, Spinal Interlaminal

GMDN Terms

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

Identifiers

Type ID
Primary 06009708426147

Customer Contacts

Phone
+27123860012

Premarket Submissions

Submission Number Supplement Number
K080075 000