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SURGICAL KIT-ACUFEX MOSAICPLASTY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962789
510(k) Type
Traditional
Applicant
SMITH & NEPHEW ENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/1996
Days to Decision
28 days
Submission Type
Summary

SURGICAL KIT-ACUFEX MOSAICPLASTY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962789
510(k) Type
Traditional
Applicant
SMITH & NEPHEW ENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/1996
Days to Decision
28 days
Submission Type
Summary