The following data is part of a premarket notification filed by Oxford Performance Materials, Inc. with the FDA for Osteofab Patient Specific Facial Device.
Device ID | K161052 |
510k Number | K161052 |
Device Name: | OsteoFab Patient Specific Facial Device |
Classification | Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction |
Applicant | OXFORD PERFORMANCE MATERIALS, INC. 30 S Satellite Road South Windsor, CT 06074 |
Contact | Leigh Ayres |
Correspondent | Leigh Ayres OXFORD PERFORMANCE MATERIALS, INC. 30 S Satellite Road South Windsor, CT 06074 |
Product Code | KKY |
CFR Regulation Number | 878.3500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-04-14 |
Decision Date | 2016-07-20 |
Summary: | summary |