FDA UDI In Commercial Distribution 🇺🇸 United States

GMK SpheriKA Cementless

DI: 07630345799340 · Model: 02.12.KA174L · Medacta International SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
GMK SpheriKA Cementless
Primary DI
07630345799340
Version / Model
02.12.KA174L
Company Name
Medacta International SA
Labeler DUNS
488227125
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-23
Public Version
1
Public Version Date
2023-01-31
Public Version Status
New
Public Device Record Key
50ac85b1-0294-40aa-9c6e-554a16fb5599

Device Description

GMK SpheriKa Femur Porous TiGrowthC+HA S4+L

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
MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

GMDN Terms

Code Name
33745 Coated knee femur prosthesis

Identifiers

Type ID
Primary 07630345799340

Premarket Submissions

Submission Number Supplement Number
K223548 000