TRUE/FLEX HUMERUS CAP
K-Number: K920598 · 1992-04-28
Advertisement
Device Summary
Frequently Asked Questions
What is the TRUE/FLEX HUMERUS CAP?
TRUE/FLEX HUMERUS CAP is a medical device that received FDA 510(k) clearance on 1992-04-28. The listed applicant is Applied Osteo Systems, Inc.. The 510(k) number is K920598.
When did TRUE/FLEX HUMERUS CAP receive FDA 510(k) clearance?
TRUE/FLEX HUMERUS CAP received FDA 510(k) clearance on 1992-04-28, under 510(k) number K920598.
Who is the listed applicant for TRUE/FLEX HUMERUS CAP?
The FDA 510(k) record lists Applied Osteo Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRUE/FLEX HUMERUS CAP?
The FDA product code for TRUE/FLEX HUMERUS CAP 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 Applied Osteo 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: 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.
Advertisement