MOSS MIAMI SPINAL SYSTEM (ANTERIOR USE)
K-Number: K953915 · 1996-02-15
Advertisement
Device Summary
Frequently Asked Questions
What is the MOSS MIAMI SPINAL SYSTEM (ANTERIOR USE)?
MOSS MIAMI SPINAL SYSTEM (ANTERIOR USE) is a medical device that received FDA 510(k) clearance on 1996-02-15. The listed applicant is Depuy, Inc.. The 510(k) number is K953915.
When did MOSS MIAMI SPINAL SYSTEM (ANTERIOR USE) receive FDA 510(k) clearance?
MOSS MIAMI SPINAL SYSTEM (ANTERIOR USE) received FDA 510(k) clearance on 1996-02-15, under 510(k) number K953915.
Who is the listed applicant for MOSS MIAMI SPINAL SYSTEM (ANTERIOR USE)?
The FDA 510(k) record lists Depuy, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOSS MIAMI SPINAL SYSTEM (ANTERIOR USE)?
The FDA product code for MOSS MIAMI SPINAL SYSTEM (ANTERIOR USE) is MNH. This falls under the ENT category.
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 Depuy, 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: MNH)
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