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SMOOTH STAPLE IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900433
510(k) Type
Traditional
Applicant
INTERPHASE IMPLANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
11/16/1990
Days to Decision
290 days

SMOOTH STAPLE IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900433
510(k) Type
Traditional
Applicant
INTERPHASE IMPLANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
11/16/1990
Days to Decision
290 days