FDA UDI In Commercial Distribution 🇺🇸 United States

LOSPA IS Spinal Fixation System

DI: 08800017253657 · Model: SA.227.7565 · Corentec Co., Ltd
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LOSPA IS Spinal Fixation System
Primary DI
08800017253657
Version / Model
SA.227.7565
Company Name
Corentec Co., Ltd
Labeler DUNS
688739895
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-14
Public Version
2
Public Version Date
2023-04-24
Public Version Status
Update
Public Device Record Key
7e12094c-e3ba-499a-bb81-a194b59a9dcc

Device Description

POLYAXIAL GUIDED PEDICLE SCREW II - Guided type Ø7.5 X 65, Length 28.2mm

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
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
NKB Thoracolumbosacral Pedicle Screw System
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

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

Identifiers

Type ID
Primary 08800017253657

Customer Contacts

Phone
+82414107176

Premarket Submissions

Submission Number Supplement Number
K200267 000