DIAO HAND SURGERY SET— 510(k) K960539

Substantially Equivalent

Kinetikos Medical, Inc.

FDA 510(k) clearance K960539 for DIAO HAND SURGERY SET, Substantially Equivalent on 1996-07-23. Applicant: Kinetikos Medical, Inc.. Device class: 1.

Clearance details

Applicant: Kinetikos Medical, Inc.
Product code: Code HXB
Device class: Class 1
Regulation: 21 CFR 888.4540
Advisory panel: Orthopedic
Date received: 1996-02-07
Decision date: 1996-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, 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.