The following data is part of a premarket notification filed by Seaspine, Inc. with the FDA for Newport Spinal System.
Device ID | K083089 |
510k Number | K083089 |
Device Name: | NEWPORT SPINAL SYSTEM |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | SEASPINE, INC. 2302 LA MIRADA DR. Vista, CA 92081 -7862 |
Contact | Ethel Bernal |
Correspondent | Ethel Bernal SEASPINE, INC. 2302 LA MIRADA DR. Vista, CA 92081 -7862 |
Product Code | NKB |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-10-16 |
Decision Date | 2009-01-13 |