FDA UDI In Commercial Distribution 🇺🇸 United States

LANCER Pedicle Screw System

DI: 00840996174183 · Model: MT30-70110 · Choice Spine, LP
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LANCER Pedicle Screw System
Primary DI
00840996174183
Version / Model
MT30-70110
Company Name
Choice Spine, LP
Labeler DUNS
078293017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-17
Public Version
1
Public Version Date
2018-09-17
Public Version Status
New
Public Device Record Key
ffed25b3-75bd-4dd0-bbd8-8398a89ec6bb

Device Description

LANCER,SCREW,POLYAXIAL,7.0X110

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
NKB Thoracolumbosacral pedicle screw system
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00840996174183

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K171456 000

Device Sizes

Type Value Unit Text
Outer Diameter 7 Millimeter
Length 110 Millimeter