FDA UDI In Commercial Distribution 🇺🇸 United States

Reform Midline Cortical Screw System

DI: 00815362025871 · Model: 59-BC-9500 · PRECISION SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reform Midline Cortical Screw System
Primary DI
00815362025871
Version / Model
59-BC-9500
Catalog Number
59-BC-9500
Company Name
PRECISION SPINE, INC.
Labeler DUNS
079398589
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-07
Public Version
1
Public Version Date
2019-05-15
Public Version Status
New
Public Device Record Key
c484ad66-8056-4688-8b43-50d2cfef0277

Device Description

Ø9.5 x 100mm Midline Cortical Bone Screw, Cannulated

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
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

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

Identifiers

Type ID
Primary 00815362025871

Premarket Submissions

Submission Number Supplement Number
K173130 000