FDA UDI In Commercial Distribution 🇺🇸 United States

Versa-Fx®

DI: 00889024037151 · Model: 1193-135-18 · Zimmer, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Versa-Fx®
Primary DI
00889024037151
Version / Model
1193-135-18
Catalog Number
00-1193-135-18
Company Name
Zimmer, Inc.
Labeler DUNS
056038268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-17
Public Version
5
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
e903c651-4973-405e-ac42-b01ebb3e5285

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
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

GMDN Terms

Code Name
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00889024037151

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K150818 000
K954555 000

Device Sizes

Type Value Unit Text
Angle 135 degree
Length 310 Millimeter
Device Size Text, specify 18 Holes