Last synced on 14 November 2025 at 11:06 pm

HITCH LACTOSORB SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K061657
510(k) Type
Traditional
Applicant
ARTHROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2006
Days to Decision
42 days
Submission Type
Summary

HITCH LACTOSORB SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K061657
510(k) Type
Traditional
Applicant
ARTHROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2006
Days to Decision
42 days
Submission Type
Summary