FDA UDI In Commercial Distribution 🇺🇸 United States

Reform Ti Modular HA Pedicle Screw System

DI: 00840019957724 · Model: 39-HMC-7540 · PRECISION SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reform Ti Modular HA Pedicle Screw System
Primary DI
00840019957724
Version / Model
39-HMC-7540
Catalog Number
39-HMC-7540
Company Name
PRECISION SPINE, INC.
Labeler DUNS
079398589
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-22
Public Version
1
Public Version Date
2022-08-01
Public Version Status
New
Public Device Record Key
b8dfdb84-5fe5-42e4-8e99-4389255165ea

Device Description

Ø7.5 mm x 40mm Modular 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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

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

Identifiers

Type ID
Primary 00840019957724

Premarket Submissions

Submission Number Supplement Number
K151422 000