The following data is part of a premarket notification filed by Medicrea International S.a. with the FDA for Pass Lp Spinal System.
Device ID | K190376 |
510k Number | K190376 |
Device Name: | PASS LP Spinal System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Medicrea International S.A. 5389 Route De Strasbourg - Vancia Rillieux-la-pape, FR 69140 |
Contact | David Ryan |
Correspondent | David Ryan Medicrea International S.A. 5389 Route De Strasbourg - Vancia Rillieux-la-pape, FR 69140 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-02-19 |
Decision Date | 2019-05-02 |