FDA UDI In Commercial Distribution 🇺🇸 United States

ICONIX

DI: 07613252450344 · Model: 3910-500-522 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ICONIX
Primary DI
07613252450344
Version / Model
3910-500-522
Catalog Number
3910-500-522
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-26
Public Version
5
Public Version Date
2019-03-21
Public Version Status
Update
Public Device Record Key
30884fe1-6eae-4adb-9505-a8844f1d0011

Device Description

2.3MM ICONIX 2 ANCHOR W/INTELLIBRAID TECHNOLOGY 2 STRANDS #2 FORCE FIBER

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
No
MRI Safety
MR Safe
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
45062 Tendon/ligament bone anchor, non-bioabsorbable

Identifiers

Type ID
Package 37613252450345
Primary 07613252450344

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K133671 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 2.3 Millimeter