FDA UDI In Commercial Distribution 🇺🇸 United States

True Spinal Fixation System

DI: B50610593072 · Model: 105-9-307 · INNOVATIVE SURGICAL DESIGNS
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
True Spinal Fixation System
Primary DI
B50610593072
Version / Model
105-9-307
Company Name
INNOVATIVE SURGICAL DESIGNS
Labeler DUNS
078306079
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-09
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d11c245e-3efb-423a-ad53-0c18c5b9e16e

Device Description

Rod Benders

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

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

Identifiers

Type ID
Primary B50610593072

Customer Contacts

Phone
8123694252

Premarket Submissions

Submission Number Supplement Number
K133690 000