CONQUEST FN

Device, Fixation, Proximal Femoral, Implant

Smith & Nephew

The following data is part of a premarket notification filed by Smith & Nephew with the FDA for Conquest Fn.

Pre-market Notification Details

• Device ID: K152686
• 510k Number: K152686
• Device Name: CONQUEST FN
• Classification: Device, Fixation, Proximal Femoral, Implant
• Applicant: Smith & Nephew 1450 E. Brooks Rd. Memphis, TN 38116
• Contact: Bradley Heil
• Correspondent: Bradley Heil; Smith & Nephew 1450 E. Brooks Rd. Memphis, TN 38116
• Product Code: JDO
• CFR Regulation Number: 888.3030 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2015-09-18
• Decision Date: 2016-03-17
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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