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

POROUS HYDROXYAPATITE BG200

K Number: K841201 · Decision Aug 3, 1984
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
225
Applicant Total
25
Review Days
135

Basic Information

Device Name
POROUS HYDROXYAPATITE BG200
K Number
K841201
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
INTERPORE INTL.
Date Received
March 21, 1984
Decision Date
August 3, 1984
Product Code
LYC
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
LYC Bone Grafting Material, Synthetic

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K960945 IMZ MEMBRANE TACK SYSTEM
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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.
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