FDA UDI In Commercial Distribution 🇺🇸 United States

LineSider

DI: 03662663098922 · Model: LS-N6ME7560 · Highridge Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LineSider
Primary DI
03662663098922
Version / Model
LS-N6ME7560
Catalog Number
LS-N6ME7560
Company Name
Highridge Medical, LLC
Labeler DUNS
119260394
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-03
Public Version
1
Public Version Date
2025-10-13
Public Version Status
New
Public Device Record Key
8abd2b99-dc96-4c5c-bcfc-c48c61ac32c6

Device Description

5.5/6.0mm, Non-mod MIS 7.1mm - Dual to Quad, Non-cannulated - 7.5mm x 60mm

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
No

Product Codes

Code Name
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 03662663098922

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K203367 000