FDA UDI In Commercial Distribution 🇺🇸 United States

Reform Pedicle Screw System

DI: 00840019901352 · Model: 39-RU-5530 · PRECISION SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reform Pedicle Screw System
Primary DI
00840019901352
Version / Model
39-RU-5530
Catalog Number
39-RU-5530
Company Name
PRECISION SPINE, INC.
Labeler DUNS
079398589
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-23
Public Version
1
Public Version Date
2019-05-31
Public Version Status
New
Public Device Record Key
0c737fd1-2437-4ee7-9ea3-65e7d553ab43

Device Description

Ø5.5mm x 30mm Reduction Uniplanar Screw

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

GMDN Terms

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

Identifiers

Type ID
Primary 00840019901352

Premarket Submissions

Submission Number Supplement Number
K121172 000