The following data is part of a premarket notification filed by Seaspine Orthopedics Corporation with the FDA for Seaspine Waveform C Interbody System.
Device ID | K212904 |
510k Number | K212904 |
Device Name: | SeaSpine WaveForm C Interbody System |
Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Applicant | SeaSpine Orthopedics Corporation 5770 Armada Drive Carlsbad, CA 92008 |
Contact | Hong Phan |
Correspondent | Aly Alvarez SeaSpine Orthopedics Corporation 5770 Armada Drive Carlsbad, CA 92008 |
Product Code | OVE |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-09-13 |
Decision Date | 2021-12-14 |