OSTEO FEMORAL NAIL
K-Number: K922195 · 1992-07-23
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Device Summary
Frequently Asked Questions
What is the OSTEO FEMORAL NAIL?
OSTEO FEMORAL NAIL is a medical device that received FDA 510(k) clearance on 1992-07-23. The listed applicant is Osteo AG. The 510(k) number is K922195.
When did OSTEO FEMORAL NAIL receive FDA 510(k) clearance?
OSTEO FEMORAL NAIL received FDA 510(k) clearance on 1992-07-23, under 510(k) number K922195.
Who is the listed applicant for OSTEO FEMORAL NAIL?
The FDA 510(k) record lists Osteo AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSTEO FEMORAL NAIL?
The FDA product code for OSTEO FEMORAL NAIL is HSB.
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 Osteo 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: HSB)
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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