FDA UDI In Commercial Distribution 🇺🇸 United States

Dymaxeon

DI: 00815500025022 · Model: 06.0 · BACK 2 BASIC DIRECT, LLC
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
Dymaxeon
Primary DI
00815500025022
Version / Model
06.0
Catalog Number
06.2130
Company Name
BACK 2 BASIC DIRECT, LLC
Labeler DUNS
043841348
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2019-03-04
Public Version
1
Public Version Date
2019-03-12
Public Version Status
New
Public Device Record Key
2cd4c194-1016-4951-ad46-f5be2ef23bf4

Device Description

DYMAXEON 6.0 MONOAXIAL PEDICLE SCREW Ø4.5 x 30mm (VIOLET)

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
MR Conditional
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NKB Thoracolumbosacral Pedicle Screw System
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00815500025022
Unit of Use 10815500025029

Customer Contacts

Phone
216-447-5025

Premarket Submissions

Submission Number Supplement Number
K121786 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 86 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
– 86 Degrees Fahrenheit