KNEE INTERPOSITIONAL MINI-REPAIR SYSTEM (KIMRS)— 510(k) K033242

Name: FDA 510(k) clearance K033242
Creator: U.S. Food and Drug Administration
Published: 2003-12-31

Substantially Equivalent

Imaging Therapeutics, Inc.

FDA 510(k) clearance K033242 for KNEE INTERPOSITIONAL MINI-REPAIR SYSTEM (KIMRS), Substantially Equivalent on 2003-12-31. Applicant: Imaging Therapeutics, Inc.. Device class: 2.

Clearance details

Applicant: Imaging Therapeutics, Inc.
Product code: Code HSH
Device class: Class 2
Regulation: 21 CFR 888.3590
Advisory panel: Orthopedic
Date received: 2003-10-07
Decision date: 2003-12-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Mateo, CA, US

Download summary PDF View on FDA.gov ↗

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