FDA UDI In Commercial Distribution 🇺🇸 United States

VIA Spinous Process Fixation System

DI: M7404400042 · Model: 34-13-02 · SPINEOLOGY INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VIA Spinous Process Fixation System
Primary DI
M7404400042
Version / Model
34-13-02
Catalog Number
440-0042
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-02-25
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
f97396f0-c7c5-4ba9-ae02-4b29dddc3dcb

Device Description

7mm Dilator

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
MR Unsafe
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
PEK Spinous process plate

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary M7404400042

Customer Contacts

Phone
+1(651)256-8500 ext. 534

Premarket Submissions

Submission Number Supplement Number
K142213 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 7
Length 7 Millimeter