FDA UDI In Commercial Distribution 🇺🇸 United States

V-TEK™

DI: 00889024110236 · Model: 28.65.110 · Zimmer GmbH
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
V-TEK™
Primary DI
00889024110236
Version / Model
28.65.110
Company Name
Zimmer GmbH
Labeler DUNS
488133448
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-30
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
1d73b622-9e89-40b2-8065-eb62a44ae2c4

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
Yes
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
HTN WASHER, BOLT NUT

GMDN Terms

Code Name
61689 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00889024110236

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K151708 000

Device Sizes

Type Value Unit Text
Outer Diameter 2 Millimeter
Device Size Text, specify TX6
Length 10 Millimeter