SurgiCase Viewer
FDA 510(k) K170419 · Materialise NV
510(k) numberK170419
Submission
- Device name
- SurgiCase Viewer
- Applicant
- Materialise NV
Leuven, BE - Received
- February 13, 2017
- Decision date
- May 11, 2017
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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Questions and answers
When was SurgiCase Viewer cleared by the FDA?
SurgiCase Viewer (K170419) received a 510(k) decision of Substantially Equivalent on May 11, 2017, 87 days after the submission was received.
What is the product code of K170419?
The FDA product code is LLZ – System, Image Processing, Radiological, a Class II (moderate risk) device regulated under 21 CFR 892.2050.