FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10885862062253 · Model: 231-04-03 · Exactech, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10885862062253
Version / Model
231-04-03
Catalog Number
231-04-03
Company Name
Exactech, Inc.
Labeler DUNS
157565946
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-28
Public Version
1
Public Version Date
2022-08-05
Public Version Status
New
Public Device Record Key
d91be72a-16d4-42dc-865e-a90284775f25

Device Description

TRIAL HANDLE, TIBIAL INSERT

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 10885862062253

Premarket Submissions

Submission Number Supplement Number
K033883 000
K093360 000
K110547 000
K111400 000
K121307 000
K123342 000
K132161 000