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ALLTHREAD LACTOSORB SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K061389
510(k) Type
Traditional
Applicant
ARTHROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2006
Days to Decision
62 days
Submission Type
Summary

ALLTHREAD LACTOSORB SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K061389
510(k) Type
Traditional
Applicant
ARTHROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2006
Days to Decision
62 days
Submission Type
Summary