The following data is part of a premarket notification filed by Howmedica Osteonics Corp. with the FDA for Profyle System.
| Device ID | K062498 | 
| 510k Number | K062498 | 
| Device Name: | PROFYLE SYSTEM | 
| Classification | Plate, Fixation, Bone | 
| Applicant | HOWMEDICA OSTEONICS CORP. 325 Corporate Drive Mahwah, NJ 07430 | 
| Contact | Vivian Kelly | 
| Correspondent | Vivian Kelly HOWMEDICA OSTEONICS CORP. 325 Corporate Drive Mahwah, NJ 07430  | 
| Product Code | HRS | 
| CFR Regulation Number | 888.3030 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2006-08-25 | 
| Decision Date | 2006-10-25 | 
| Summary: | summary |