FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

NEW ALLEN IMPLANT

K Number: K900081 · Decision Mar 23, 1990
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
38
Applicant Total
12
Review Days
78

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Basic Information

Device Name
NEW ALLEN IMPLANT
K Number
K900081
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.3320
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Oculo Plastik, Inc.
Date Received
January 4, 1990
Decision Date
March 23, 1990
Product Code
HPZ
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HPZ Implant, Eye Sphere

Similar 510(k) Clearances

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Other Clearances by Oculo Plastik, Inc.

K Number Device Name
K112176 SILICONE SPHERES
K073293 DURETTE IMPLANT
K040689 EYE SPHERE IMPLANTS
K934834 EPTFE SHEET COVERING FOR OCULAR IMPLANT
K915630 OPHTIMPLANT
K901002 O'DONNELL, SOCKET RECONSTRUCTION PROSTHESES
K900929 PUTTERMAN-SCOTT, SOCKET RECONSTRUCTION BILATERAL
K900928 COX MALAR EMINENCE IMPLANTS
K900927 CODERE-DURETTE ORBITAL FLOOR IMPLANT
K900930 SPIVEY-ALLEN ORBITAL FLOOR IMPLANT
Search all 12 clearances from Oculo Plastik, Inc. →