TITANIUM MODULAR COLLARED HIP PROSTHESIS
K-Number: K895035 · 1990-01-31
Advertisement
Device Summary
Frequently Asked Questions
What is the TITANIUM MODULAR COLLARED HIP PROSTHESIS?
TITANIUM MODULAR COLLARED HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1990-01-31. The listed applicant is Depuy, Inc.. The 510(k) number is K895035.
When did TITANIUM MODULAR COLLARED HIP PROSTHESIS receive FDA 510(k) clearance?
TITANIUM MODULAR COLLARED HIP PROSTHESIS received FDA 510(k) clearance on 1990-01-31, under 510(k) number K895035.
Who is the listed applicant for TITANIUM MODULAR COLLARED HIP PROSTHESIS?
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 TITANIUM MODULAR COLLARED HIP PROSTHESIS?
The FDA product code for TITANIUM MODULAR COLLARED HIP PROSTHESIS is JDI.
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: JDI)
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