ZIMMER BONE CEMENT CENTRIFUGATION SYS
K-Number: K843219 · 1984-11-29
Advertisement
Device Summary
Frequently Asked Questions
What is the ZIMMER BONE CEMENT CENTRIFUGATION SYS?
ZIMMER BONE CEMENT CENTRIFUGATION SYS is a medical device that received FDA 510(k) clearance on 1984-11-29. The listed applicant is Zimmer, Inc.. The 510(k) number is K843219.
When did ZIMMER BONE CEMENT CENTRIFUGATION SYS receive FDA 510(k) clearance?
ZIMMER BONE CEMENT CENTRIFUGATION SYS received FDA 510(k) clearance on 1984-11-29, under 510(k) number K843219.
Who is the listed applicant for ZIMMER BONE CEMENT CENTRIFUGATION SYS?
The FDA 510(k) record lists Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZIMMER BONE CEMENT CENTRIFUGATION SYS?
The FDA product code for ZIMMER BONE CEMENT CENTRIFUGATION SYS is JDZ.
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 Zimmer, 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: JDZ)
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