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 |