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TWINFIX ULTRA TI, TWINFIX ULTRA PK, TWINFIX ULTRA HA SUTURE ANCHORS

Page Type
Cleared 510(K)
510(k) Number
K112526
510(k) Type
Traditional
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2012
Days to Decision
153 days
Submission Type
Summary

TWINFIX ULTRA TI, TWINFIX ULTRA PK, TWINFIX ULTRA HA SUTURE ANCHORS

Page Type
Cleared 510(K)
510(k) Number
K112526
510(k) Type
Traditional
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2012
Days to Decision
153 days
Submission Type
Summary