REVISION HIP SYSTEM

Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented

SMITH & NEPHEW RICHARDS, INC.

The following data is part of a premarket notification filed by Smith & Nephew Richards, Inc. with the FDA for Revision Hip System.

Pre-market Notification Details

• Device ID: K963486
• 510k Number: K963486
• Device Name: REVISION HIP SYSTEM
• Classification: Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented
• Applicant: SMITH & NEPHEW RICHARDS, INC. 1450 E. BROOKS RD. Memphis, TN 38116
• Contact: Thomas L Craig
• Correspondent: Thomas L Craig; SMITH & NEPHEW RICHARDS, INC. 1450 E. BROOKS RD. Memphis, TN 38116
• Product Code: JDI
• CFR Regulation Number: 888.3350 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1996-09-03
• Decision Date: 1996-11-27
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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03596010479303	K963486	000
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