FEMUR WRENCH
K-Number: K870126 · 1987-02-03
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Device Summary
Frequently Asked Questions
What is the FEMUR WRENCH?
FEMUR WRENCH is a medical device that received FDA 510(k) clearance on 1987-02-03. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K870126.
When did FEMUR WRENCH receive FDA 510(k) clearance?
FEMUR WRENCH received FDA 510(k) clearance on 1987-02-03, under 510(k) number K870126.
Who is the listed applicant for FEMUR WRENCH?
The FDA 510(k) record lists Orthopedic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FEMUR WRENCH?
The FDA product code for FEMUR WRENCH is GEG.
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 Orthopedic Systems, Inc. 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: GEG)
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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