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ULTRASLIDE ACROMIOCLAVICULAR AND SYNDESMOTIC REPAIR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K082095
510(k) Type
Traditional
Applicant
SMITH & NEPHEW ENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2008
Days to Decision
89 days
Submission Type
Summary

ULTRASLIDE ACROMIOCLAVICULAR AND SYNDESMOTIC REPAIR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K082095
510(k) Type
Traditional
Applicant
SMITH & NEPHEW ENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2008
Days to Decision
89 days
Submission Type
Summary