FDA UDI In Commercial Distribution 🇺🇸 United States

XULTAN COUINTER TORQ

DI: 00819824023764 · Model: 1029-03-1000 ASSY · MET 1 TECHNOLOGIES, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
XULTAN COUINTER TORQ
Primary DI
00819824023764
Version / Model
1029-03-1000 ASSY
Catalog Number
1029-03-1000 ASSY
Company Name
MET 1 TECHNOLOGIES, LLC
Labeler DUNS
080474650
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-29
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
838ad392-e173-4ea0-89d6-bd8f408a54eb

Device Description

THE XULTAN 5.5 PEDICLE SCREW SYSTEM IS AN IMPLANT DEVICE MANUFACTURED FROM TITANIUM AND SILICONE. THE SCREWS ARE AVAILABLE CANNULATED OR NON-CANNULATED IN VARIOUS DIAMETERS AND LENGTHS TO ACCOMMODATE VARIOUS PATIENT ANATOMIES. THE SYSTEM INCLUDES STRAIGHT RODS, CURVED RODS, CROSSLINKS, AND ASSOCIATED INSTRUMENTATION.

Device Characteristics

Single Use
No
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
No
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
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

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

Identifiers

Type ID
Primary 00819824023764

Customer Contacts

Phone
9154726762

Premarket Submissions

Submission Number Supplement Number
K170108 000