Last synced on 18 April 2025 at 11:05 pm

IMTEC SENDAX MDI AND MDI PLUS ENDOSSEOUS IMPLANT, MODELS OB-XX, SH-XX, MOB-22, MSH-XX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031106
510(k) Type
Traditional
Applicant
IMTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2003
Days to Decision
126 days
Submission Type
Statement

IMTEC SENDAX MDI AND MDI PLUS ENDOSSEOUS IMPLANT, MODELS OB-XX, SH-XX, MOB-22, MSH-XX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031106
510(k) Type
Traditional
Applicant
IMTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2003
Days to Decision
126 days
Submission Type
Statement