The following data is part of a premarket notification filed by Zavation Llc with the FDA for Zavation Spinal System.
Device ID | K112484 |
510k Number | K112484 |
Device Name: | ZAVATION SPINAL SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | ZAVATION LLC 501 AVALON WAY Brandon, MS 39047 |
Contact | John Walker |
Correspondent | John Walker ZAVATION LLC 501 AVALON WAY Brandon, MS 39047 |
Product Code | MNI |
Subsequent Product Code | KWP |
Subsequent Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-08-29 |
Decision Date | 2011-11-22 |
Summary: | summary |