S2 POSTERIOR-TIB— 510(k) K832296

Substantially Equivalent

Anstek Corp.

FDA 510(k) clearance K832296 for S2 POSTERIOR-TIB, Substantially Equivalent on 1983-08-31. Applicant: Anstek Corp..

Clearance details

Applicant: Anstek Corp.
Product code: Code GXY
Advisory panel: Neurology
Date received: 1983-07-13
Decision date: 1983-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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