Last synced on 25 April 2025 at 11:05 pm

AccelFix Lumbar Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192481
510(k) Type
Traditional
Applicant
L&K Biomed Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/28/2020
Days to Decision
322 days
Submission Type
Summary

AccelFix Lumbar Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192481
510(k) Type
Traditional
Applicant
L&K Biomed Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/28/2020
Days to Decision
322 days
Submission Type
Summary