The following data is part of a premarket notification filed by Ldr Spine Usa with the FDA for Ldr Spine Usa Spine Tune Tl Spine System.
Device ID | K100575 |
510k Number | K100575 |
Device Name: | LDR SPINE USA SPINE TUNE TL SPINE SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | LDR SPINE USA 4030 WEST BRAKER LANE SUITE 360 Austin, TX 78759 |
Contact | Noah Bartsch |
Correspondent | Noah Bartsch LDR SPINE USA 4030 WEST BRAKER LANE SUITE 360 Austin, TX 78759 |
Product Code | MNI |
Subsequent Product Code | KWP |
Subsequent Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-03-01 |
Decision Date | 2010-03-31 |
Summary: | summary |