FDA · official record K052471Substantially Equivalent

HDC SPIDER SCREW

Name: HDC SPIDER SCREW — FDA K052471
Creator: Hdc S.R.L.
Keywords: HDC SPIDER SCREW, HDC SPIDER SCREW, K052471, DZE, FDA

United StatesDZEHdc S.R.L.

Verified

Official record identity

FDA application number: K052471
Decision date: December 23, 2005
Published decision: Substantially Equivalent

Classification

Product code: DZE

Published parties

Applicant: Hdc S.R.L.

Additional source fields

Decision code: SESE
Published decision: Substantially Equivalent
Submission type: Traditional
Received date: 2005-09-08
Review panel: Dental
Current product-code class (harmonized): 2
Current product-code regulation (harmonized): 872.3640

About this record

This record preserves an application published in the FDA 510(k) bulk export, including the DEN entries FDA includes in that export. Historical decisions do not establish current marketing status. Product-code harmonization is separate from the original application; joined establishment identifiers are not assigned to the applicant. The complete official export is checked daily and raw evidence is retained.