FDA UDI In Commercial Distribution 🇺🇸 United States

Biomet SpinalPak Non-invasive Spine Fusion Stimulator System

DI: 00812301020218 · Model: 1067716 · EBI, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Biomet SpinalPak Non-invasive Spine Fusion Stimulator System
Primary DI
00812301020218
Version / Model
1067716
Catalog Number
1067716
Company Name
EBI, LLC
Labeler DUNS
050410323
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-19
Public Version
4
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
b7c156a8-f27f-4310-b9f7-b9a1a06e07a9

Device Description

SPINALPAK ASSEMBLY

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LOF Stimulator, Bone Growth, Non-Invasive

GMDN Terms

Code Name
35463 Patient-worn bone growth electromagnetic stimulator

Identifiers

Type ID
Primary 00812301020218

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P850022 017

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 100 KiloPascal
Type
Special Storage Condition, Specify
Special Conditions
Keep Dry
Type
Storage Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
5 – 122 Degrees Fahrenheit