Materialise N.V.
4 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| ProPlan CMF Patient-Specific Guide, Mandible guides (3A & 3B)-Intended to guide the markin recall (Z-2287-2023) | Materialise N.V. | 2023-08-03 |
| MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instrumen recall (Z-2213-2023) | Materialise N.V. | 2023-07-20 |
| Signature Patient-Specific Surgical Guides; patient specific instruments used as a guide d recall (Z-0162-2016) | Materialise N.V. | 2015-10-23 |
| Signature TKA GDE/MDL Set 04-05 (Femur & Tibia) The Signature Patient-Specific Surgical Gu recall (Z-1287-2015) | Materialise N.V. | 2015-03-17 |
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Every clearance here is in the API, with alerts when new ones post.