Last synced on 30 May 2025 at 11:05 pm

BIORC ANCHOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990770
510(k) Type
Traditional
Applicant
LINVATEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1999
Days to Decision
143 days
Submission Type
Summary

BIORC ANCHOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990770
510(k) Type
Traditional
Applicant
LINVATEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1999
Days to Decision
143 days
Submission Type
Summary