FDA UDI In Commercial Distribution 🇺🇸 United States

Reform HA Coated Pedicle Screw System

DI: 00815362020562 · Model: 39-PH-1055 · PRECISION SPINE, INC.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reform HA Coated Pedicle Screw System
Primary DI
00815362020562
Version / Model
39-PH-1055
Catalog Number
39-PH-1055
Company Name
PRECISION SPINE, INC.
Labeler DUNS
079398589
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-28
Public Version
2
Public Version Date
2019-08-08
Public Version Status
Update
Public Device Record Key
42f0b64a-bd59-4e2c-bd41-3e134b1074a7

Device Description

10.5 x 55mm Reform HA Coated Pedicle Screw System

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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation
NKB Thoracolumbosacral Pedicle Screw System
OSH Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis
KWP Appliance, Fixation, Spinal Interlaminal

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00815362020562

Premarket Submissions

Submission Number Supplement Number
K151422 000