TITANIUM STAPLES
K-Number: K890841 · 1989-04-19
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Device Summary
Frequently Asked Questions
What is the TITANIUM STAPLES?
TITANIUM STAPLES is a medical device that received FDA 510(k) clearance on 1989-04-19. The listed applicant is ETHICON, Inc.. The 510(k) number is K890841.
When did TITANIUM STAPLES receive FDA 510(k) clearance?
TITANIUM STAPLES received FDA 510(k) clearance on 1989-04-19, under 510(k) number K890841.
Who is the listed applicant for TITANIUM STAPLES?
The FDA 510(k) record lists ETHICON, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TITANIUM STAPLES?
The FDA product code for TITANIUM STAPLES is GDW.
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 ETHICON, 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: GDW)
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.
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