FDA UDI In Commercial Distribution 🇺🇸 United States

DynaFORCE™ HiMax

DI: 00815432028146 · Model: DynaFORCE HiMAX Single Packaged Implant 20mm x 14mm x 14mm · CROSSROADS EXTREMITY SYSTEMS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DynaFORCE™ HiMax
Primary DI
00815432028146
Version / Model
DynaFORCE HiMAX Single Packaged Implant 20mm x 14mm x 14mm
Catalog Number
7120-1414
Company Name
CROSSROADS EXTREMITY SYSTEMS
Labeler DUNS
058864308
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-20
Public Version
2
Public Version Date
2021-11-23
Public Version Status
Update
Public Device Record Key
5d9bfab0-4c18-469e-a43e-a04fdd13d5c3

Device Description

DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JDR Staple, Fixation, Bone

GMDN Terms

Code Name
61669 Orthopaedic bone staple, non-adjustable

Identifiers

Type ID
Primary 00815432028146

Customer Contacts

Phone
901-221-8406