ACE UNIVERSAL RECONSTRUCTION PLATE
K-Number: K930592 · 1993-07-26
Advertisement
Device Summary
Frequently Asked Questions
What is the ACE UNIVERSAL RECONSTRUCTION PLATE?
ACE UNIVERSAL RECONSTRUCTION PLATE is a medical device that received FDA 510(k) clearance on 1993-07-26. The listed applicant is Ace Medical Co.. The 510(k) number is K930592.
When did ACE UNIVERSAL RECONSTRUCTION PLATE receive FDA 510(k) clearance?
ACE UNIVERSAL RECONSTRUCTION PLATE received FDA 510(k) clearance on 1993-07-26, under 510(k) number K930592.
Who is the listed applicant for ACE UNIVERSAL RECONSTRUCTION PLATE?
The FDA 510(k) record lists Ace Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACE UNIVERSAL RECONSTRUCTION PLATE?
The FDA product code for ACE UNIVERSAL RECONSTRUCTION PLATE is HRS.
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 Ace Medical Co. 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: HRS)
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