Last synced on 14 November 2025 at 11:06 pm

LRTM SURGICAL MESH

Page Type
Cleared 510(K)
510(k) Number
K070560
510(k) Type
Traditional
Applicant
LIFECELL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2007
Days to Decision
104 days
Submission Type
Summary

LRTM SURGICAL MESH

Page Type
Cleared 510(K)
510(k) Number
K070560
510(k) Type
Traditional
Applicant
LIFECELL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2007
Days to Decision
104 days
Submission Type
Summary