FDA UDI In Commercial Distribution 🇺🇸 United States

STRoPP

DI: 00815432023783 · Model: STRoPP Plantar Plate Repair Kit - Sterile · CROSSROADS EXTREMITY SYSTEMS
Product Codes
1
GMDN Terms
7
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
STRoPP
Primary DI
00815432023783
Version / Model
STRoPP Plantar Plate Repair Kit - Sterile
Catalog Number
1601-0002
Company Name
CROSSROADS EXTREMITY SYSTEMS
Labeler DUNS
058864308
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-05
Public Version
14
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
8e7df9f4-f642-49fe-a5f9-2cb79173fb86

Device Description

The STROPP (Single Tunnel Repair of Plantar Plate) System is a sterile packaged kit that include PEEK implants and related instruments for plantar plate repair. Implants are packaged with the following manual surgical instruments for general use: a needle, needle passer, suture passer, an inserter, K-wires and distractor. The implants are compatible with Size 0 suture; suture is not included with the system. The STROPP System is intended for use with a suture in metatarsal ligament and tendon repairs.

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
MBI Fastener, Fixation, Nondegradable, Soft Tissue

GMDN Terms

Code Name
61143 Suturing needle, single-use
57874 Suturing unit, single-use
35685 Orthopaedic bone wire
61807 Bone-resection orthopaedic reamer, single-use
61806 Bone-resection orthopaedic reamer, reprocessed
45062 Tendon/ligament bone anchor, non-bioabsorbable
47568 Suturing needle holder, single-use

Identifiers

Type ID
Primary 00815432023783

Customer Contacts

Phone
901-221-8406

Device Sizes

Type Value Unit Text
Device Size Text, specify 3.0mm Diameter x 8.0mm Length