VARIAX 2 COMPRESSION PLATING SYSTEM
K-Number: K130009 · 2013-03-22
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Device Summary
Frequently Asked Questions
What is the VARIAX 2 COMPRESSION PLATING SYSTEM?
VARIAX 2 COMPRESSION PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2013-03-22. The listed applicant is Stryker Trauma AG. The 510(k) number is K130009.
When did VARIAX 2 COMPRESSION PLATING SYSTEM receive FDA 510(k) clearance?
VARIAX 2 COMPRESSION PLATING SYSTEM received FDA 510(k) clearance on 2013-03-22, under 510(k) number K130009.
Who is the listed applicant for VARIAX 2 COMPRESSION PLATING SYSTEM?
The FDA 510(k) record lists Stryker Trauma AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VARIAX 2 COMPRESSION PLATING SYSTEM?
The FDA product code for VARIAX 2 COMPRESSION PLATING SYSTEM 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 Stryker Trauma AG 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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