The following data is part of a premarket notification filed by Zavation, Llc with the FDA for Zavation Posterior Leif.
Device ID | K142392 |
510k Number | K142392 |
Device Name: | Zavation Posterior LEIF |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | ZAVATION, LLC 400 LIBERTY PARK Flowood, MS 39232 |
Contact | Lawerence Walker |
Correspondent | Lawerence Walker ZAVATION, LLC 400 LIBERTY PARK Flowood, MS 39232 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-08-27 |
Decision Date | 2015-04-29 |
Summary: | summary |