SPINALPLANE— 510(k) K934336

Name: FDA 510(k) clearance K934336
Creator: U.S. Food and Drug Administration
Published: 1995-03-10

Substantially Equivalent for Some Indications

Synvasive Technology, Inc.

FDA 510(k) clearance K934336 for SPINALPLANE, Substantially Equivalent for Some Indications on 1995-03-10. Applicant: Synvasive Technology, Inc.. Device class: 1.

Clearance details

Applicant: Synvasive Technology, Inc.
Product code: Code HSZ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1993-09-07
Decision date: 1995-03-10
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Rancho Cordova, CA, US

Download summary PDF View on FDA.gov ↗

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