SYNTHES LCP PEDIATRIC PLATE SYSTEMS
K-Number: K112085 · 2011-11-17
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Device Summary
Frequently Asked Questions
What is the SYNTHES LCP PEDIATRIC PLATE SYSTEMS?
SYNTHES LCP PEDIATRIC PLATE SYSTEMS is a medical device that received FDA 510(k) clearance on 2011-11-17. The listed applicant is Synthes (USA) Products, LLC. The 510(k) number is K112085.
When did SYNTHES LCP PEDIATRIC PLATE SYSTEMS receive FDA 510(k) clearance?
SYNTHES LCP PEDIATRIC PLATE SYSTEMS received FDA 510(k) clearance on 2011-11-17, under 510(k) number K112085.
Who is the listed applicant for SYNTHES LCP PEDIATRIC PLATE SYSTEMS?
The FDA 510(k) record lists Synthes (USA) Products, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTHES LCP PEDIATRIC PLATE SYSTEMS?
The FDA product code for SYNTHES LCP PEDIATRIC PLATE SYSTEMS is HRS.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Synthes (USA) Products, LLC as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HRS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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