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IMPLANTECH TEMPORAL IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K943644
510(k) Type
Traditional
Applicant
IMPLANTECH ASSOCIATES, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
10/18/1994
Days to Decision
83 days
Submission Type
Statement

IMPLANTECH TEMPORAL IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K943644
510(k) Type
Traditional
Applicant
IMPLANTECH ASSOCIATES, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
10/18/1994
Days to Decision
83 days
Submission Type
Statement