TITANIUM/STAINLESS STEEL INSTRUMENTS
K-Number: K902911 · 1990-09-06
Advertisement
Device Summary
Frequently Asked Questions
What is the TITANIUM/STAINLESS STEEL INSTRUMENTS?
TITANIUM/STAINLESS STEEL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1990-09-06. The listed applicant is Impla-Med. The 510(k) number is K902911.
When did TITANIUM/STAINLESS STEEL INSTRUMENTS receive FDA 510(k) clearance?
TITANIUM/STAINLESS STEEL INSTRUMENTS received FDA 510(k) clearance on 1990-09-06, under 510(k) number K902911.
Who is the listed applicant for TITANIUM/STAINLESS STEEL INSTRUMENTS?
The FDA 510(k) record lists Impla-Med as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TITANIUM/STAINLESS STEEL INSTRUMENTS?
The FDA product code for TITANIUM/STAINLESS STEEL INSTRUMENTS is DZE.
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 Impla-Med 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: DZE)
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