Last synced on 6 June 2025 at 11:06 pm

MOBIO Total Knee System Posterior Stabilized (PS and PS+) Tibial Inserts, MOBIO Total Knee System Patellar Component

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183025
510(k) Type
Traditional
Applicant
b-One Ortho Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2019
Days to Decision
88 days
Submission Type
Summary

MOBIO Total Knee System Posterior Stabilized (PS and PS+) Tibial Inserts, MOBIO Total Knee System Patellar Component

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183025
510(k) Type
Traditional
Applicant
b-One Ortho Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2019
Days to Decision
88 days
Submission Type
Summary