FDA UDI In Commercial Distribution 🇺🇸 United States

Adaptix™ Interbody System with Titan nanoLOCK™ Surface Technology

DI: 00763000202927 · Model: 84332413 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Adaptix™ Interbody System with Titan nanoLOCK™ Surface Technology
Primary DI
00763000202927
Version / Model
84332413
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-04
Public Version
1
Public Version Date
2020-10-12
Public Version Status
New
Public Device Record Key
fee32521-8024-4e3f-bd58-48a4d6c39596

Device Description

SPACER 84332413 ADAPTIX 24MM X 13MM

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
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
No
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
43084 Intervertebral-body internal spinal fixation system

Identifiers

Type ID
Primary 00763000202927

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K201267 000