Oxford Performance Materials

FDA Filings

This page includes the latest FDA filings for Oxford Performance Materials. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

Registration Number	3009582362
FEI Number	3009582362
Name	OXFORD PERFORMANCE MATERIALS
Owner & Operator	Oxford Performance Materials
Contact Address	30 South Satellite Road South Windsor CT 06074 US
Official Correspondent	Beth Pashko x-860-6569450-x
Registration Status	1
Initial Importer	N
Registration Expiration	2020-04-25
Registration Address	30 South Satellite Road South Windsor, CT 06074 US
Establishment Type	Complaint File Establishment per 21 CFR 820.198

FDA Filings

Device Company	Device	Date
HWJ OXFORD PERFORMANCE MATERIALS	OsteoFab Suture Anchor Awls	2019-12-10
PMN K190915 \| MBI OXFORD PERFORMANCE MATERIALS	OsteoFab Suture Anchors	2019-08-19
PMN K180064 \| GXN OXFORD PERFORMANCE MATERIALS	OsteoFab Patient Specific Cranial Device	2019-05-16
PMN K161052 \| KKY OXFORD PERFORMANCE MATERIALS	OsteoFab Patient Specific Facial Device - Optimized	2016-08-19
PMN K161052 \| KKY OXFORD PERFORMANCE MATERIALS	HTR-PEKK-Optimized	2016-08-19
PMN K142005 \| MQP OXFORD PERFORMANCE MATERIALS	SpineFab? VBR	2015-08-31
PMN K142005 OXFORD PERFORMANCE MATERIALS	SpineFab Vertebral Body Replacement (VBR) System	2015-07-10
PMN K133809 \| KKY OXFORD PERFORMANCE MATERIALS	OsteoFab Patient Specific Facial Device	2014-10-29
PMN K133809 \| KKY OXFORD PERFORMANCE MATERIALS	HTR-PEKK	2014-10-29
PMN K133809 OXFORD PERFORMANCE MATERIALS	OSTEOFAB PATIENT SPECIFIC FACIAL DEVICE	2014-07-28
PMN K121818 \| GXN OXFORD PERFORMANCE MATERIALS	OsteoFab Patient Specific Cranial Device	2013-02-20
PMN K121818 \| GXN OXFORD PERFORMANCE MATERIALS	HTR-PEKK	2013-02-20
PMN K121818 OXFORD PERFORMANCE MATERIALS	OSTEOFAB PATIENT SPECIFIC CRANIAL DEVICE	2013-02-07

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