FDA UDI In Commercial Distribution 🇺🇸 United States

P-LIFT®

DI: 00190361003045 · Model: 01-06014-12 · SPINEFRONTIER, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
P-LIFT®
Primary DI
00190361003045
Version / Model
01-06014-12
Company Name
SPINEFRONTIER, INC.
Labeler DUNS
002003243
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-15
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
4d64e86e-e32a-43a9-8a57-483280a58981

Device Description

P-LIFT, Straight, CONED, 8W X 27L X 12H

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

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 00190361003045

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K111553 000

Device Sizes

Type Value Unit Text
Length 27 Millimeter
Width 8 Millimeter
Height 12 Millimeter