The following data is part of a premarket notification filed by Kelyniam Global, Inc with the FDA for Kelyniam Custom Skull Implant (csi).
Device ID | K103582 |
510k Number | K103582 |
Device Name: | KELYNIAM CUSTOM SKULL IMPLANT (CSI) |
Classification | Plate, Cranioplasty, Preformed, Non-alterable |
Applicant | KELYNIAM GLOBAL, INC 200 MYRTLE STREET 2ND FLOOR New Britain, CT 06053 |
Contact | James Ketner |
Correspondent | James Ketner KELYNIAM GLOBAL, INC 200 MYRTLE STREET 2ND FLOOR New Britain, CT 06053 |
Product Code | GXN |
CFR Regulation Number | 882.5330 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-12-08 |
Decision Date | 2011-04-14 |
Summary: | summary |