FDA UDI In Commercial Distribution 🇺🇸 United States

PYXIS 3D Titanium Cervical Cage System

DI: 08800322709603 · Model: GS136-0527P · GS Medical Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PYXIS 3D Titanium Cervical Cage System
Primary DI
08800322709603
Version / Model
GS136-0527P
Catalog Number
GS136-0527P
Company Name
GS Medical Co., Ltd.
Labeler DUNS
688385418
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-18
Public Version
1
Public Version Date
2025-07-28
Public Version Status
New
Public Device Record Key
f652e2da-b082-4618-aafa-c3c38e76da06

Device Description

Cervical Trial

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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 08800322709603

Customer Contacts

Phone
+82432377393

Premarket Submissions

Submission Number Supplement Number
K221687 000