The following data is part of a premarket notification filed by Zimmer Trabecular Metal Technology with the FDA for Vista-s Device, Associated Instrumentation.
Device ID | K133784 |
510k Number | K133784 |
Device Name: | VISTA-S DEVICE, ASSOCIATED INSTRUMENTATION |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | ZIMMER TRABECULAR METAL TECHNOLOGY 10 POMEROY RD. Parsippany, NJ 07054 |
Contact | Judith Rosen |
Correspondent | Judith Rosen ZIMMER TRABECULAR METAL TECHNOLOGY 10 POMEROY RD. Parsippany, NJ 07054 |
Product Code | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-12-12 |
Decision Date | 2014-07-07 |
Summary: | summary |