Osteocentric Trauma L L C

FDA Filings

This page includes the latest FDA filings for Osteocentric Trauma L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3011656326
• FEI Number: 3011656326
• Name: OsteoCentric Trauma, LLC
• Owner & Operator: OsteoCentric Trauma, LLC
• Contact Address: 5113 Southwest Parkway Suite 150 ; Austin TX 78735 US
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 5113 Southwest Pkwy, Ste 150 ; Austin, TX 78735 US
• Establishment Type: Complaint File Establishment per 21 CFR 820.198

FDA Filings

Device Company	Device	Date
PMN K190430 | HWC OsteoCentric Trauma, LLC	OsteoCentric Bone Plate and Screw System	2019-03-29
PMN K190430 | HRS OsteoCentric Trauma, LLC	OsteoCentric Bone Plate and Screw System	2019-03-29
PMN K182171 | JDW OsteoCentric Trauma, LLC	SMV Scientific K-Wire and Pins	2019-03-29
PMN K182171 | HTY OsteoCentric Trauma, LLC	SMV Scientific K-Wire and Pins	2019-03-29
PMN K170021 | HWC OsteoCentric Trauma, LLC	OsteoCentric Trauma Cannulated Bone Screw Fastener System	2018-07-18
PMN K160946 | HWC OsteoCentric Trauma, LLC	OsteoCentric Trauma Cancellous Bone Screw Fastener System	2018-07-18
PMN K160946 | HTN OsteoCentric Trauma, LLC	OsteoCentric Trauma Cancellous Bone Screw Fastener System	2018-07-18
PMN K160603 | HWC OsteoCentric Trauma, LLC	OsteoCentric Trauma Schanz Screw	2016-03-29
PMN K152000 | HWC OsteoCentric Trauma, LLC	OsteoCentric Trauma Plate and Screw System	2015-12-03
PMN K152000 | HRS OsteoCentric Trauma, LLC	OsteoCentric Trauma Plate and Screw System	2015-12-03
PMN K150981 | HWC OsteoCentric Trauma, LLC	OsteoCentric Trauma Bone Screw	2015-12-03
PMN K150188 | HWC OsteoCentric Trauma, LLC	OsteoCentric Trauma Bone Fastener	2015-06-10