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 |