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SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K093897
510(k) Type
Traditional
Applicant
SMITH & NEPHEW INC., ENDOSCOPY DIV.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2010
Days to Decision
76 days
Submission Type
Summary

SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K093897
510(k) Type
Traditional
Applicant
SMITH & NEPHEW INC., ENDOSCOPY DIV.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2010
Days to Decision
76 days
Submission Type
Summary