The following data is part of a premarket notification filed by Precision Spine, Inc. with the FDA for Reform Pedicle Screw System.
Device ID | K151422 |
510k Number | K151422 |
Device Name: | Reform Pedicle Screw System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Precision Spine, Inc. 2050 Executive Drive Pearl, MS 39208 |
Contact | Michael C. Dawson |
Correspondent | Michael C. Dawson Precision Spine, Inc. 2050 Executive Drive Pearl, MS 39208 |
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 | 2015-05-28 |
Decision Date | 2015-08-21 |
Summary: | summary |