FDA UDI Not in Commercial Distribution 🇺🇸 United States

Forefoot

DI: 10381780064398 · Model: FFINSTSET · NEWDEAL
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Forefoot
Primary DI
10381780064398
Version / Model
FFINSTSET
Catalog Number
FFINSTSET
Company Name
NEWDEAL
Labeler DUNS
536935331
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-22
Public Version
6
Public Version Date
2023-05-22
Public Version Status
Update
Public Device Record Key
c33f8248-beed-49f1-ad30-210515bd0227
Distribution End Date
2023-03-31

Device Description

The principal of the FOREFOOT sets is to propose a group of implants (screws and staples) and the associated instruments in a single package dedicated to the forefoot orthopaedic surgery. The set is intended to make easy the surgeon work and give more solution in the same set. The Forefoot Set includes Bold compression screws, QWIX fixation screws, Spin snap-off screws, Solustaple, Uni-clip staples, and instrumentation.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
HTY PIN, FIXATION, SMOOTH
HWC Screw, fixation, bone
JDR STAPLE, FIXATION, BONE

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 10381780064398
Secondary M248FFINSTSET1

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in dry place.