FDA UDI In Commercial Distribution 🇺🇸 United States

MD-Max ULIF

DI: 00840019914765 · Model: 43-7000-7525 · PRECISION SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MD-Max ULIF
Primary DI
00840019914765
Version / Model
43-7000-7525
Catalog Number
43-7000-7525
Company Name
PRECISION SPINE, INC.
Labeler DUNS
079398589
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-10
Public Version
1
Public Version Date
2019-05-20
Public Version Status
New
Public Device Record Key
46bd24c9-1806-4abe-a7ca-36fde147aa19

Device Description

Ø7.5 Extended Tab Screw 25mm

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
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
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

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

Identifiers

Type ID
Primary 00840019914765

Premarket Submissions

Submission Number Supplement Number
K122931 000