MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT
K-Number: K062004 · 2006-08-15
Advertisement
Device Summary
Frequently Asked Questions
What is the MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT?
MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT is a medical device that received FDA 510(k) clearance on 2006-08-15. The listed applicant is Quantum Orthopedics, Inc.. The 510(k) number is K062004.
When did MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT receive FDA 510(k) clearance?
MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT received FDA 510(k) clearance on 2006-08-15, under 510(k) number K062004.
Who is the listed applicant for MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT?
The FDA 510(k) record lists Quantum Orthopedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT?
The FDA product code for MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT is MQP.
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 Quantum Orthopedics, 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: MQP)
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