The following data is part of a premarket notification filed by Medicrea International with the FDA for Pass Lp Spinal System.
Device ID | K140738 |
510k Number | K140738 |
Device Name: | PASS LP SPINAL SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | MEDICREA INTERNATIONAL 14 PORTE DU GRAND LYON Neyron, FR 01700 |
Contact | David Ryan |
Correspondent | David Ryan MEDICREA INTERNATIONAL 14 PORTE DU GRAND LYON Neyron, FR 01700 |
Product Code | MNI |
Subsequent Product Code | KWP |
Subsequent Product Code | MNH |
Subsequent Product Code | OSH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-03-25 |
Decision Date | 2014-11-04 |
Summary: | summary |