Last synced on 18 April 2025 at 11:05 pm

LL Implant System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242379
510(k) Type
Traditional
Applicant
Ossvis Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
11/7/2024
Days to Decision
87 days
Submission Type
Summary

LL Implant System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242379
510(k) Type
Traditional
Applicant
Ossvis Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
11/7/2024
Days to Decision
87 days
Submission Type
Summary