SYNTHES (USA) TROCHANTER STABILIZATION PLATE FOR DHS
K-Number: K000972 · 2000-06-16
Advertisement
Device Summary
Frequently Asked Questions
What is the SYNTHES (USA) TROCHANTER STABILIZATION PLATE FOR DHS?
SYNTHES (USA) TROCHANTER STABILIZATION PLATE FOR DHS is a medical device that received FDA 510(k) clearance on 2000-06-16. The listed applicant is Synthes (Usa). The 510(k) number is K000972.
When did SYNTHES (USA) TROCHANTER STABILIZATION PLATE FOR DHS receive FDA 510(k) clearance?
SYNTHES (USA) TROCHANTER STABILIZATION PLATE FOR DHS received FDA 510(k) clearance on 2000-06-16, under 510(k) number K000972.
Who is the listed applicant for SYNTHES (USA) TROCHANTER STABILIZATION PLATE FOR DHS?
The FDA 510(k) record lists Synthes (Usa) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTHES (USA) TROCHANTER STABILIZATION PLATE FOR DHS?
The FDA product code for SYNTHES (USA) TROCHANTER STABILIZATION PLATE FOR DHS is LXT.
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 Synthes (Usa) 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: LXT)
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