FDA UDI In Commercial Distribution 🇺🇸 United States

PedFuse®

DI: 00190361015000 · Model: 01-80187-25 · SPINEFRONTIER, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PedFuse®
Primary DI
00190361015000
Version / Model
01-80187-25
Company Name
SPINEFRONTIER, INC.
Labeler DUNS
002003243
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-15
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
9602370d-087e-4b02-8ff7-a455a2ca8c50

Device Description

Screw Assy REset Cann 6.0X25mm Gen 3

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
Yes
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
MNH Orthosis, spondylolisthesis spinal fixation
MNI ORTHOSIS, SPINAL PEDICLE FIXATION

GMDN Terms

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

Identifiers

Type ID
Primary 00190361015000

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123164 000

Device Sizes

Type Value Unit Text
Length 25 Millimeter
Outer Diameter 6 Millimeter