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 | K161627 |
510k Number | K161627 |
Device Name: | PASS LP Spinal System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | MEDICREA INTERNATIONAL S.A. 14 PORTE DU GRAND LYON Neyron, FR 01700 |
Contact | David Ryan |
Correspondent | David Ryan MEDICREA INTERNATIONAL S.A. 14 PORTE DU GRAND LYON Neyron, FR 01700 |
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 | 2016-06-13 |
Decision Date | 2016-07-29 |
Summary: | summary |