FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH

K Number: K901928 · Decision Jul 26, 1990
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
23
Applicant Total
25
Review Days
90

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Basic Information

Device Name
INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH
K Number
K901928
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.3165
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Interpore Intl.
Date Received
April 27, 1990
Decision Date
July 26, 1990
Product Code
EGG
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
EGG Attachment, Precision, All

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Other Clearances by Interpore Intl.

K Number Device Name
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K972842 INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE
K971036 ODONTIT AUTOGENOUS BONE COLLECTION DEVICE
K960945 IMZ MEMBRANE TACK SYSTEM
K960371 INTERPORE THREADED IMPLANT
K955492 INTERPORE IMZ CYL IMPLANT & CYL HEX IMPLT
K952167 IMZ BONE TACK SYSTEM
K950165 INTERPORE IP 200 GRANULAR CORALLINE HYDROXYAPATITE BONE VOID FILLERS, 425 TO 1000 MICRONS AND 425 TO 600 MICRONS
K922872 INTERPORE CYLINDRICAL HEX HYDROXYAPATITE COATED IMPLANT, 3.3 MM DIAM.
Search all 25 clearances from Interpore Intl. →