Colorado Therapeutics Xenograft Implant
K-Number: K172937 · 2017-10-25
Device Summary
Frequently Asked Questions
What is the Colorado Therapeutics Xenograft Implant?
Colorado Therapeutics Xenograft Implant is a medical device that received FDA 510(k) clearance on 2017-10-25. The listed applicant is Colorado Therapeutics, LLC. The 510(k) number is K172937.
When did Colorado Therapeutics Xenograft Implant receive FDA 510(k) clearance?
Colorado Therapeutics Xenograft Implant received FDA 510(k) clearance on 2017-10-25, under 510(k) number K172937.
Who is the listed applicant for Colorado Therapeutics Xenograft Implant?
The FDA 510(k) record lists Colorado Therapeutics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Colorado Therapeutics Xenograft Implant?
The FDA product code for Colorado Therapeutics Xenograft Implant is FTM.
Other records listing Colorado Therapeutics, LLC 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: FTM)
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.