OSTEOGEN (HA RESORB)— 510(k) K923310

Substantially Equivalent

Impladent

FDA 510(k) clearance K923310 for OSTEOGEN (HA RESORB), Substantially Equivalent on 1995-05-31. Applicant: Impladent. Device class: 2.

Clearance details

Applicant: Impladent
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 1992-07-07
Decision date: 1995-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hollis, NY, US

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More clearances from Impladent

K881662 — EXPANDED CLAIMES TO OSTEOGEN(R)1988-09-01
K843398 — OSTEOGEN1984-12-27
K812321 — HYDROXI-FLEX IMPLANT1981-10-29
K792663 — FLEXI-CUP IMPLANT1980-01-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.