The following data is part of a premarket notification filed by Spr Therapeutics, Inc. with the FDA for Sprint Pns System.
| Device ID | K211801 |
| 510k Number | K211801 |
| Device Name: | SPRINT PNS System |
| Classification | Stimulator, Nerve, Electrical, Percutaneous (pens), For Pain Relief |
| Applicant | SPR Therapeutics, Inc. 22901 Millcreek Blvd. Suite 110 Cleveland, OH 44122 |
| Contact | Kathryn Stager |
| Correspondent | Kathryn Stager SPR Therapeutics, Inc. 22901 Millcreek Blvd. Suite 110 Cleveland, OH 44122 |
| Product Code | NHI |
| CFR Regulation Number | 882.5890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-06-10 |
| Decision Date | 2021-10-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SPRINT PNS SYSTEM 98514555 not registered Live/Pending |
SPR Therapeutics, Inc. 2024-04-23 |