FDA UDI In Commercial Distribution 🇺🇸 United States

Reform POCT System

DI: 00840019967945 · Model: 55-PM-4035 · PRECISION SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reform POCT System
Primary DI
00840019967945
Version / Model
55-PM-4035
Catalog Number
55-PM-4035
Company Name
PRECISION SPINE, INC.
Labeler DUNS
079398589
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-22
Public Version
1
Public Version Date
2022-11-30
Public Version Status
New
Public Device Record Key
d640ad78-12c6-4700-ba0f-2d1ab2c7cd97

Device Description

Ø4.0 x 35mm Polyaxial Screw - M/L Bias

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
Yes
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
Yes
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
NKG Posterior Cervical Screw System
KWP Appliance, Fixation, Spinal Interlaminal

GMDN Terms

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

Identifiers

Type ID
Primary 00840019967945

Premarket Submissions

Submission Number Supplement Number
K162300 000