SYNTHES 2.7 MM/3.5 MM LCP DISTAL FIBULA PLATES

Plate, Fixation, Bone

SYNTHES (USA)

The following data is part of a premarket notification filed by Synthes (usa) with the FDA for Synthes 2.7 Mm/3.5 Mm Lcp Distal Fibula Plates.

Pre-market Notification Details

• Device ID: K073460
• 510k Number: K073460
• Device Name: SYNTHES 2.7 MM/3.5 MM LCP DISTAL FIBULA PLATES
• Classification: Plate, Fixation, Bone
• Applicant: SYNTHES (USA) 1301 GOSHEN PKWY West Chester, PA 19380
• Contact: Sheri L Musgnung
• Correspondent: Sheri L Musgnung; SYNTHES (USA) 1301 GOSHEN PKWY West Chester, PA 19380
• Product Code: HRS
• CFR Regulation Number: 888.3030 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2007-12-10
• Decision Date: 2008-02-21
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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