IMPLARETTE— 510(k) K911655

Name: FDA 510(k) clearance K911655
Creator: U.S. Food and Drug Administration
Published: 1991-10-21

Substantially Equivalent

Implant Innovations International, Inc.

FDA 510(k) clearance K911655 for IMPLARETTE, Substantially Equivalent on 1991-10-21. Applicant: Implant Innovations International, Inc.. Device class: 1.

Clearance details

Applicant: Implant Innovations International, Inc.
Product code: Code EKJ
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1991-04-12
Decision date: 1991-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Palm Beach, FL, US

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K945077 — INSTRUMENT,FILLING,PLASTIC,DENTAL1994-11-30

More clearances from Implant Innovations International, Inc.

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K935544 — 3I STANDARD THREADED/SELF-TAPPING THREADED IMPLANTS MODIFICATION1995-03-13
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K905303 — ABUTMENT GLO1991-06-10
K911701 — G-FLOSS & G-FLOSS II1991-05-15
K891613 — OVERDENTURE ATTACHMENT1989-10-10

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