The following data is part of a premarket notification filed by Medos International Sarl with the FDA for Codman Certas Programmable Valve System.
Device ID | K113526 |
510k Number | K113526 |
Device Name: | CODMAN CERTAS PROGRAMMABLE VALVE SYSTEM |
Classification | Shunt, Central Nervous System And Components |
Applicant | MEDOS INTERNATIONAL SARL 325 Paramount Drive Raynham, MA 02767 |
Contact | Jocelyn Raposo |
Correspondent | Jocelyn Raposo MEDOS INTERNATIONAL SARL 325 Paramount Drive Raynham, MA 02767 |
Product Code | JXG |
CFR Regulation Number | 882.5550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-11-30 |
Decision Date | 2012-02-16 |
Summary: | summary |