TRANSJAW(TM)— 510(k) K872815

Substantially Equivalent

Vitek, Inc.

FDA 510(k) clearance K872815 for TRANSJAW(TM), Substantially Equivalent on 1988-01-19. Applicant: Vitek, Inc.. Device class: 1.

Clearance details

Applicant: Vitek, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1987-07-16
Decision date: 1988-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, 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.