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MODIFICATION OF PROLENE (POLYPROPYLENE) HERNIA SYSTEM, NONABSORBABLE SYNTHETIC SURGICAL MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984220
510(k) Type
Traditional
Applicant
ETHICON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1999
Days to Decision
90 days
Submission Type
Summary

MODIFICATION OF PROLENE (POLYPROPYLENE) HERNIA SYSTEM, NONABSORBABLE SYNTHETIC SURGICAL MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984220
510(k) Type
Traditional
Applicant
ETHICON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1999
Days to Decision
90 days
Submission Type
Summary