FDA UDI In Commercial Distribution 🇺🇸 United States

Reform POCT System

DI: 00840019937009 · Model: 55-BK-0103 · PRECISION SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reform POCT System
Primary DI
00840019937009
Version / Model
55-BK-0103
Catalog Number
55-BK-0103
Company Name
PRECISION SPINE, INC.
Labeler DUNS
079398589
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-30
Public Version
1
Public Version Date
2019-09-09
Public Version Status
New
Public Device Record Key
32ecab34-ed5c-4837-8c37-1b42296c4a7a

Device Description

Occipital Implant Kit

Device Characteristics

Single Use
No
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
KWP Appliance, Fixation, Spinal Interlaminal
NKG Posterior Cervical Screw System

GMDN Terms

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

Identifiers

Type ID
Primary 00840019937009

Premarket Submissions

Submission Number Supplement Number
K162300 000
K172495 000