FDA UDI In Commercial Distribution 🇺🇸 United States

PIVOX™ Oblique Lateral Spinal System

DI: 00763000385941 · Model: X0220058 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
PIVOX™ Oblique Lateral Spinal System
Primary DI
00763000385941
Version / Model
X0220058
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
2
Public Version Date
2021-04-21
Public Version Status
Update
Public Device Record Key
7743a424-331d-4daf-9d5a-fd1fc88cd354

Device Description

INSERTER X0220058 PIVOX 25 DEGREE

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 00763000385941

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K152277 000