The following data is part of a premarket notification filed by Seaspine, Inc. with the FDA for Zuma, Model 55-xxxx/56-xxxx.
Device ID | K082926 |
510k Number | K082926 |
Device Name: | ZUMA, MODEL 55-XXXX/56-XXXX |
Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Applicant | SEASPINE, INC. 2302 LA MIRADA DR. Vista, CA 92081 -7862 |
Contact | Jeff Brittan |
Correspondent | Jeff Brittan SEASPINE, INC. 2302 LA MIRADA DR. Vista, CA 92081 -7862 |
Product Code | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-10-01 |
Decision Date | 2008-12-22 |
Summary: | summary |