K213587 is an FDA 510(k) clearance for the MyCRO Band. This device is classified as a Orthosis, Cranial (Class II - Special Controls, product code MVA).
Submitted by Otto Bock Healthcare LP (Salt Lake City, US). The FDA issued a Cleared decision on June 9, 2022, 209 days after receiving the submission on November 12, 2021.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.5970.
| 510(k) Number | K213587 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 12, 2021 |
| Decision Date | June 09, 2022 |
| Days to Decision | 209 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Summary PDF |
| Product Code | MVA — Orthosis, Cranial |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 882.5970 |