FDA UDI In Commercial Distribution 🇺🇸 United States

Equinoxe®

DI: 10885862625656 · Model: 320-55-07 · Exactech, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Equinoxe®
Primary DI
10885862625656
Version / Model
320-55-07
Catalog Number
320-55-07
Company Name
Exactech, Inc.
Labeler DUNS
157565946
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-13
Public Version
1
Public Version Date
2024-08-21
Public Version Status
New
Public Device Record Key
a8a12535-b183-4ca1-b3b7-6fe0deb31cd3

Device Description

Central Screw Baseplate

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PHX shoulder prosthesis, reverse configuration
KWT PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED

GMDN Terms

Code Name
48091 Reverse shoulder prosthesis base plate

Identifiers

Type ID
Primary 10885862625656

Premarket Submissions

Submission Number Supplement Number
K233482 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Left
Device Size Text, specify Posterior/Superior Augment
Device Size Text, specify 8/10 Degree