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IMPLANTECH JEJ PERI-PYRIFORM IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962824
510(k) Type
Traditional
Applicant
IMPLANTECH ASSOCIATES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/1996
Days to Decision
76 days
Submission Type
Statement

IMPLANTECH JEJ PERI-PYRIFORM IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962824
510(k) Type
Traditional
Applicant
IMPLANTECH ASSOCIATES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/1996
Days to Decision
76 days
Submission Type
Statement