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 |