VersaWrap Nerve Protector (VTP-2201); VersaWrap Nerve Protector (VTP-1201)
K-Number: K251175 · 2025-07-17
Device Summary
Frequently Asked Questions
What is the VersaWrap Nerve Protector (VTP-2201); VersaWrap Nerve Protector (VTP-1201)?
VersaWrap Nerve Protector (VTP-2201); VersaWrap Nerve Protector (VTP-1201) is a medical device that received FDA 510(k) clearance on 2025-07-17. The listed applicant is Alafair Biosciences. The 510(k) number is K251175.
When did VersaWrap Nerve Protector (VTP-2201); VersaWrap Nerve Protector (VTP-1201) receive FDA 510(k) clearance?
VersaWrap Nerve Protector (VTP-2201); VersaWrap Nerve Protector (VTP-1201) received FDA 510(k) clearance on 2025-07-17, under 510(k) number K251175.
Who is the listed applicant for VersaWrap Nerve Protector (VTP-2201); VersaWrap Nerve Protector (VTP-1201)?
The FDA 510(k) record lists Alafair Biosciences as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VersaWrap Nerve Protector (VTP-2201); VersaWrap Nerve Protector (VTP-1201)?
The FDA product code for VersaWrap Nerve Protector (VTP-2201); VersaWrap Nerve Protector (VTP-1201) is JXI.
Other records listing Alafair Biosciences 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: JXI)
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.