FDA UDI In Commercial Distribution 🇺🇸 United States

LineSider

DI: 00818613021950 · Model: LS-SC7A8555 · Integrity Implants Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LineSider
Primary DI
00818613021950
Version / Model
LS-SC7A8555
Catalog Number
LS-SC7A8555
Company Name
Integrity Implants Inc.
Labeler DUNS
080300717
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-20
Public Version
3
Public Version Date
2022-05-13
Public Version Status
Update
Public Device Record Key
8e7ff43f-5ef4-448f-a8e2-9596a96119a6

Device Description

Dual Lead Shank - Non-Cannulated - 7.1mm Ball 8.5mm x 55mm

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
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWP Appliance, Fixation, Spinal Interlaminal
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

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

Identifiers

Type ID
Primary 00818613021950

Customer Contacts

Phone
800.201.9300

Premarket Submissions

Submission Number Supplement Number
K190360 000