UROTAC BONE ANCHOR INSERTER
K-Number: K962372 · 1996-08-19
Advertisement
Device Summary
Frequently Asked Questions
What is the UROTAC BONE ANCHOR INSERTER?
UROTAC BONE ANCHOR INSERTER is a medical device that received FDA 510(k) clearance on 1996-08-19. The listed applicant is Influence, Inc.. The 510(k) number is K962372.
When did UROTAC BONE ANCHOR INSERTER receive FDA 510(k) clearance?
UROTAC BONE ANCHOR INSERTER received FDA 510(k) clearance on 1996-08-19, under 510(k) number K962372.
Who is the listed applicant for UROTAC BONE ANCHOR INSERTER?
The FDA 510(k) record lists Influence, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UROTAC BONE ANCHOR INSERTER?
The FDA product code for UROTAC BONE ANCHOR INSERTER is HXJ.
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 Influence, 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: HXJ)
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