FLEXION DISTRATION SUPPORT
K-Number: K921711 · 1992-07-13
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Device Summary
Frequently Asked Questions
What is the FLEXION DISTRATION SUPPORT?
FLEXION DISTRATION SUPPORT is a medical device that received FDA 510(k) clearance on 1992-07-13. The listed applicant is Altoona Medical Supply. The 510(k) number is K921711.
When did FLEXION DISTRATION SUPPORT receive FDA 510(k) clearance?
FLEXION DISTRATION SUPPORT received FDA 510(k) clearance on 1992-07-13, under 510(k) number K921711.
Who is the listed applicant for FLEXION DISTRATION SUPPORT?
The FDA 510(k) record lists Altoona Medical Supply as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXION DISTRATION SUPPORT?
The FDA product code for FLEXION DISTRATION SUPPORT is ILZ.
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 Altoona Medical Supply 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: ILZ)
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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