FDA UDI Not in Commercial Distribution 🇺🇸 United States

ForeFoot STP

DI: 00846832063208 · Model: FHS-010-25-30L · TORNIER, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ForeFoot STP
Primary DI
00846832063208
Version / Model
FHS-010-25-30L
Catalog Number
FHS-010-25-30L
Company Name
TORNIER, INC.
Labeler DUNS
968990812
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-16
Public Version
5
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
a7ef5ba2-5129-4b57-b361-b3a9d5cae813
Distribution End Date
2023-04-27

Device Description

Cannulated Headless Screw

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
Yes
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
HWC Screw, fixation, bone

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00846832063208

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 2.5 Millimeter
Length 30 Millimeter