Bone Mill Bone Grinder
FDA 510(k) K842845 · Acromed Corp.
510(k) numberK842845
Submission
- Device name
- Bone Mill Bone Grinder
- Applicant
- Acromed Corp.
Cleveland, OH, US - Received
- July 20, 1984
- Decision date
- October 25, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Acromed Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K980485 | Isola Spinal SystemMNI · Traditional | 10/21/1998SE |
| K981714 | Timx Low Back System Titanium MX Rod Based Low Back SystemMNH · Traditional | 06/30/1998SE |
| K981113 | Pediatric PRCMNH · Traditional | 05/29/1998SE |
| K981274 | Acromed Timx Plate Based Low Back SystemMNH · Special | 04/29/1998SE |
| K980228 | University Plate Anterior SystemKWQ · Traditional | 04/14/1998SN |
| K974757 | Kaneda Anterior Scoliosis System KassKWQ · Traditional | 03/05/1998SN |
| K972718 | M-2 Anterior Plate SystemKWQ · Traditional | 10/01/1997SN |
| K971248 | Kaneda SR Anterior Spinal SystemKWQ · Traditional | 06/11/1997SN |
| K970955 | Acromed Anterior Cervical Stabilization SystemKWQ · Traditional | 06/11/1997SN |
| K970950 | Easy RodMNH · Traditional | 06/03/1997SE |
Questions and answers
When was Bone Mill Bone Grinder cleared by the FDA?
Bone Mill Bone Grinder (K842845) received a 510(k) decision of Substantially Equivalent on October 25, 1984, 97 days after the submission was received.