Last synced on 30 May 2025 at 11:05 pm

OVOMotion Shoulder Arthroplasty System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173964
510(k) Type
Traditional
Applicant
Arthrosurface, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2018
Days to Decision
110 days
Submission Type
Summary

OVOMotion Shoulder Arthroplasty System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173964
510(k) Type
Traditional
Applicant
Arthrosurface, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2018
Days to Decision
110 days
Submission Type
Summary