FDA UDI In Commercial Distribution 🇺🇸 United States

APEX Spine System

DI: M82460008011 · Model: 6000-801 · SPINECRAFT, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
APEX Spine System
Primary DI
M82460008011
Version / Model
6000-801
Catalog Number
6000-801
Company Name
SPINECRAFT, LLC
Labeler DUNS
783908713
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-10
Public Version
1
Public Version Date
2019-01-10
Public Version Status
New
Public Device Record Key
768c0af2-e76a-4477-9adf-1833422178d4

Device Description

Vertebral Derotator Post

Device Characteristics

Single Use
No
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
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary M82460008011

Customer Contacts