FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

IMZ MEMBRANE TACK SYSTEM

K Number: K960945 · Decision May 24, 1996
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
79
Applicant Total
25
Review Days
77

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Basic Information

Device Name
IMZ MEMBRANE TACK SYSTEM
K Number
K960945
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4880
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Interpore Intl.
Date Received
March 8, 1996
Decision Date
May 24, 1996
Product Code
DZL
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
DZL Screw, Fixation, Intraosseous

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Other Clearances by Interpore Intl.

K Number Device Name
K981253 ULTRACON ULTRAFILTRATOR
K980817 PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30L
K972842 INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE
K971036 ODONTIT AUTOGENOUS BONE COLLECTION DEVICE
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.
K922732 INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER
Search all 25 clearances from Interpore Intl. →