ORTHOPLUG SOFT BONE DESIGN— 510(k) K955632

Substantially Equivalent

Sunmed, Inc.

FDA 510(k) clearance K955632 for ORTHOPLUG SOFT BONE DESIGN, Substantially Equivalent on 1996-02-27. Applicant: Sunmed, Inc.. Device class: 2.

Clearance details

Applicant: Sunmed, Inc.
Product code: Code LZN
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1995-12-11
Decision date: 1996-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redding, 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.