The following data is part of a premarket notification filed by Republic Spine, L.l.c. with the FDA for Republic Spine Dark Star Spinal System.
Device ID | K181495 |
510k Number | K181495 |
Device Name: | Republic Spine Dark Star Spinal System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Republic Spine, L.L.C. 350 Camino Gardens Blvd. Suite 103 Boca Raton, FL 33432 |
Contact | James Doulgeris |
Correspondent | James Doulgeris Republic Spine, L.L.C. 350 Camino Gardens Blvd. Suite 103 Boca Raton, FL 33432 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-06-06 |
Decision Date | 2018-07-25 |
Summary: | summary |