FDA UDI Not in Commercial Distribution 🇺🇸 United States

DynaForce

DI: 00810112597585 · Model: DynaForce, Standard Inserter, 12mm · CROSSROADS EXTREMITY SYSTEMS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
DynaForce
Primary DI
00810112597585
Version / Model
DynaForce, Standard Inserter, 12mm
Catalog Number
245104PKG
Company Name
CROSSROADS EXTREMITY SYSTEMS
Labeler DUNS
058864308
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-07
Public Version
3
Public Version Date
2024-09-11
Public Version Status
Update
Public Device Record Key
b4982fec-0a38-492d-a7c8-3c9be619ea38
Distribution End Date
2024-08-22

Device Description

DynaForce, Standard Inserter, 12mm

Device Characteristics

Single Use
No
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
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
JDR Staple, Fixation, Bone

GMDN Terms

Code Name
12696 Orthopaedic inorganic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00810112597585

Premarket Submissions

Submission Number Supplement Number
K181410 000