UROTAC BONE ANCHOR INSERTER— 510(k) K962372

Substantially Equivalent

Influence, Inc.

FDA 510(k) clearance K962372 for UROTAC BONE ANCHOR INSERTER, Substantially Equivalent on 1996-08-19. Applicant: Influence, Inc.. Device class: 1.

Clearance details

Applicant: Influence, Inc.
Product code: Code HXJ
Device class: Class 1
Regulation: 21 CFR 888.4540
Advisory panel: Orthopedic
Date received: 1996-06-19
Decision date: 1996-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.