FDA UDI In Commercial Distribution 🇺🇸 United States

AnyPlus Cervical PEEK Cage System

DI: 08806378344799 · Model: 1182-5407 · GS Medical Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AnyPlus Cervical PEEK Cage System
Primary DI
08806378344799
Version / Model
1182-5407
Catalog Number
1182-5407
Company Name
GS Medical Co., Ltd.
Labeler DUNS
688385418
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-30
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
6055a712-b145-4947-83c2-6262e2ba0ef9

Device Description

The GS Medical AnyPlus® Cervical PEEK Cage device is designed for restoring the height of the intervertebral space after resection of the disc. AnyPlus® Cervical PEEK Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The intervertebral body fusion devices are made of poly-ether-ether-ketone (PEEK Optima LT1) body with the X-ray (radio-opaque) markers made of Tantalum. The AnyPlus® Cervical PEEK Cage devices are radiolucent allowing X-ray visualization to verify device placement. AnyPlus® Cervical PEEK Cage device is supplied non-sterile and is intended for single use only. AnyPlus® Cervical PEEK Cage is designed for interbody stabilization of the cervical spine.

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
Yes
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 08806378344799

Customer Contacts

Phone
+82432377393

Premarket Submissions

Submission Number Supplement Number
K153517 000