The following data is part of a premarket notification filed by Kalitec Medical, Llc with the FDA for Tiwave-l Porous Titanium Lumbar Cage.
Device ID | K182210 |
510k Number | K182210 |
Device Name: | TiWAVE-L Porous Titanium Lumbar Cage |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | Kalitec Medical, LLC 617 E. South Street, Suite 500 Orlando, FL 32801 |
Contact | Scott Winn |
Correspondent | J.d. Webb The OrthoMedix Group, Inc. 1001 Oakwood Blvd Round Rock, TX 78681 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-08-15 |
Decision Date | 2019-01-07 |
Summary: | summary |