510(k) K201873 ยท PZR Percutaneous Nerve Stimulator For Opioid Withdrawal
Sparrow Therapy System
| Applicant | Spark Biomedical, Inc., Dallas TX, US |
| Decision | Substantially Equivalent, Jan 2, 2021 |
| Received | Jul 7, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201873
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.