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LABELING FOR MYO/WIRE II STERNOTOMY SUTURES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932513
510(k) Type
Traditional
Applicant
ALTO DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1994
Days to Decision
227 days
Submission Type
Statement

LABELING FOR MYO/WIRE II STERNOTOMY SUTURES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932513
510(k) Type
Traditional
Applicant
ALTO DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1994
Days to Decision
227 days
Submission Type
Statement