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SUTURE RETENTION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883299
510(k) Type
Traditional
Applicant
EDWARDS ORTHOPAEDICS DIV., BAXTER HEALTHCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/1988
Days to Decision
19 days

SUTURE RETENTION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883299
510(k) Type
Traditional
Applicant
EDWARDS ORTHOPAEDICS DIV., BAXTER HEALTHCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/1988
Days to Decision
19 days