KIRSCHNER SUPER-FIXATION SYSTEM
K-Number: K881896 · 1988-07-28
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Device Summary
Frequently Asked Questions
What is the KIRSCHNER SUPER-FIXATION SYSTEM?
KIRSCHNER SUPER-FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K881896.
When did KIRSCHNER SUPER-FIXATION SYSTEM receive FDA 510(k) clearance?
KIRSCHNER SUPER-FIXATION SYSTEM received FDA 510(k) clearance on 1988-07-28, under 510(k) number K881896.
Who is the listed applicant for KIRSCHNER SUPER-FIXATION SYSTEM?
The FDA 510(k) record lists Kirschner Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KIRSCHNER SUPER-FIXATION SYSTEM?
The FDA product code for KIRSCHNER SUPER-FIXATION SYSTEM is JEC.
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 Kirschner Medical Corp. 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: JEC)
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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