The following data is part of a premarket notification filed by Signature Orthopaedics Pty Ltd. with the FDA for Noosa Anterior Lumbar Plate System;nambucca Anterior Lumbar Plate System; Cairns Anterior Lumbar Plate System.
Device ID | K163625 |
510k Number | K163625 |
Device Name: | NOOSA Anterior Lumbar Plate System;NAMBUCCA Anterior Lumbar Plate System; CAIRNS Anterior Lumbar Plate System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | Signature Orthopaedics Pty Ltd. 7 Sirius Road Lane Cove, AU 2066 |
Contact | Declan Brazil |
Correspondent | Declan Brazil Signature Orthopaedics Pty Ltd. 7 Sirius Road Lane Cove, AU 2066 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-12-22 |
Decision Date | 2017-08-11 |
Summary: | summary |