Anthogyr Implanteo Implantology and Dental Surgical Motor Unit
FDA 510(k) K102241 · Anthogyr Sas
510(k) numberK102241
Submission
- Device name
- Anthogyr Implanteo Implantology and Dental Surgical Motor Unit
- Applicant
- Anthogyr Sas
Sallanches, FR - Received
- August 9, 2010
- Decision date
- March 23, 2011
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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| K160730 | Instrument kitsKCT · Traditional | 04/27/2017SE |
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| K131066 | Axiom RegDZE · Traditional | 02/21/2014SE |
| K111532 | Montblanc Surgical Contra-Angle and Straight HandpieceEGS · Traditional | 10/07/2011SE |
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Questions and answers
When was Anthogyr Implanteo Implantology and Dental Surgical Motor Unit cleared by the FDA?
Anthogyr Implanteo Implantology and Dental Surgical Motor Unit (K102241) received a 510(k) decision of Substantially Equivalent on March 23, 2011, 226 days after the submission was received.
What is the product code of K102241?
The FDA product code is EBW – Controller, Foot, Handpiece And Cord, a Class I (low risk) device regulated under 21 CFR 872.4200.