FDA UDI In Commercial Distribution 🇺🇸 United States

APEX Spine System

DI: 00193082005206 · Model: M6-6240 · SPINECRAFT, LLC
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
APEX Spine System
Primary DI
00193082005206
Version / Model
M6-6240
Catalog Number
M6-6240
Company Name
SPINECRAFT, LLC
Labeler DUNS
783908713
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-25
Public Version
1
Public Version Date
2019-04-02
Public Version Status
New
Public Device Record Key
9ab3530a-6191-4551-95c1-0852e0b677cd

Device Description

APEX Ti Mono Screw Dia.6.25, 40mm

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
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
NKB Thoracolumbosacral pedicle screw system
MNI Orthosis, spinal pedicle fixation
KWQ Appliance, fixation, spinal intervertebral body
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MNH Orthosis, spondylolisthesis spinal fixation

GMDN Terms

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

Identifiers

Type ID
Primary 00193082005206

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K062513 000
K092825 000
K102488 000
K110906 000
K132603 000