PERIARTICULAR LOCKING PLATES AND SCREWS, 2358, 2359 SERIES

Plate, Fixation, Bone

ZIMMER, INC.

The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Periarticular Locking Plates And Screws, 2358, 2359 Series.

Pre-market Notification Details

• Device ID: K040593
• 510k Number: K040593
• Device Name: PERIARTICULAR LOCKING PLATES AND SCREWS, 2358, 2359 SERIES
• Classification: Plate, Fixation, Bone
• Applicant: ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708
• Contact: Laura D Williams
• Correspondent: Laura D Williams; ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708
• Product Code: HRS
• CFR Regulation Number: 888.3030 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2004-03-08
• Decision Date: 2004-04-12
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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