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9I ORAL/MAXILLOFACIAL BONE FIXATION SYSTEM: BONE MESH-PLATE & SCREWS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953386
510(k) Type
Traditional
Applicant
IMPLANT INNOVATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1995
Days to Decision
58 days
Submission Type
Statement

9I ORAL/MAXILLOFACIAL BONE FIXATION SYSTEM: BONE MESH-PLATE & SCREWS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953386
510(k) Type
Traditional
Applicant
IMPLANT INNOVATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1995
Days to Decision
58 days
Submission Type
Statement