The following data is part of a premarket notification filed by Orthopediatrics Corp. with the FDA for Response 5.5/6.0 Spine System.
| Device ID | K150600 |
| 510k Number | K150600 |
| Device Name: | Response 5.5/6.0 Spine System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | ORTHOPEDIATRICS CORP. 2850 FRONTIER DRIVE Warsaw, IL 46582 |
| Contact | Mark Fox |
| Correspondent | Mark Fox ORTHOPEDIATRICS CORP. 2850 Frontier Drive Warsaw, IN 46582 |
| Product Code | NKB |
| Subsequent Product Code | KWP |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| Subsequent Product Code | OSH |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-03-10 |
| Decision Date | 2015-05-22 |
| Summary: | summary |