FDA UDI Not in Commercial Distribution 🇺🇸 United States

spineEOS rod Template

DI: 03700757200766 · Model: KIT0704 · ONEFIT MEDICAL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
spineEOS rod Template
Primary DI
03700757200766
Version / Model
KIT0704
Catalog Number
/
Company Name
ONEFIT MEDICAL
Labeler DUNS
263373588
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-23
Public Version
4
Public Version Date
2021-02-02
Public Version Status
Update
Public Device Record Key
63629a11-9dd1-4564-82ab-6fe4192bce1d
Distribution End Date
2021-02-01

Device Description

spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software. This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience.

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
Yes
Has Serial Number
No
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
HWT Template

GMDN Terms

Code Name
58804 Surgical implant template, single-use

Identifiers

Type ID
Primary 03700757200766

Customer Contacts

Phone
+33381252427