The following data is part of a premarket notification filed by Signature Orthopaedics Pty Ltd. with the FDA for Brisbane Alif Device, Gladstone Alif Device.
Device ID | K172019 |
510k Number | K172019 |
Device Name: | Brisbane ALIF Device, Gladstone ALIF Device |
Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
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 | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-07-05 |
Decision Date | 2017-11-29 |
Summary: | summary |