FDA UDI In Commercial Distribution 🇺🇸 United States

Titanium IntraLine

DI: 07613154890071 · Model: 3910-400-055 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Titanium IntraLine
Primary DI
07613154890071
Version / Model
3910-400-055
Catalog Number
3910-400-055
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-04
Public Version
5
Public Version Date
2019-03-21
Public Version Status
Update
Public Device Record Key
75b594dd-70fa-4943-b91b-52af074c43b4

Device Description

5.5MM TITANIUM INTRALINE ANCHOR WITH ¿ CIRCLE TAPER NEEDLES, 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
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
HWC Screw, fixation, bone

GMDN Terms

Code Name
45062 Tendon/ligament bone anchor, non-bioabsorbable

Identifiers

Type ID
Primary 07613154890071

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K071157 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 5.5 Millimeter