FDA UDI In Commercial Distribution 🇺🇸 United States

Aries-TS

DI: B06212000701 · Model: 1200-0701 · Osseus Fusion Systems, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aries-TS
Primary DI
B06212000701
Version / Model
1200-0701
Catalog Number
1200-0701
Company Name
Osseus Fusion Systems, LLC
Labeler DUNS
933442068
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-22
Public Version
1
Public Version Date
2021-12-30
Public Version Status
New
Public Device Record Key
d94471bd-9db4-4e8c-9a86-6d09e4e10e6f

Device Description

10x36x08, 0 Deg, Sterile, TLIF Interbody, Aries-TS

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary B06212000701

Premarket Submissions

Submission Number Supplement Number
K181347 000