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SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE

Page Type
Cleared 510(K)
510(k) Number
K091207
510(k) Type
Traditional
Applicant
SURGICRAFT LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2011
Days to Decision
662 days
Submission Type
Summary

SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE

Page Type
Cleared 510(K)
510(k) Number
K091207
510(k) Type
Traditional
Applicant
SURGICRAFT LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2011
Days to Decision
662 days
Submission Type
Summary