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

SPECTRUM DESIGNS PRE-FORM CONTOUR SILICONE CARVING BLOCK

K Number: K982688 · Decision Oct 13, 1998
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
44
Applicant Total
18
Review Days
71

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Basic Information

Device Name
SPECTRUM DESIGNS PRE-FORM CONTOUR SILICONE CARVING BLOCK
K Number
K982688
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spectrum Designs, Inc.
Date Received
August 3, 1998
Decision Date
October 13, 1998
Product Code
MIB
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
MIB Elastomer, Silicone Block

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Other Clearances by Spectrum Designs, Inc.

K Number Device Name
K992522 SPECTRUM DESIGNS SPECTRAGEL
K980462 SPECTRUM DESIGNS ANATOMICAL CHIN IMPLANT
K980446 SPECTRUM DESIGNS ANTERIOR CHIN IMPLANT
K980444 SPECTRUM DESIGNS BILATERAL GROOVE CHIN IMPLANT
K980463 SPECTRUM DESIGNS CURVILINEAR CHIN IMPLANT
K980445 SPECTRUM DESIGNS CONCAVE BACK CHIN IMPLANT
K980138 SPECTRUM DESIGNS SYMMETRICAL CHIN IMPLANT
K980461 SPECTRUM DESIGNS CLEFT CHIN IMPLANT
K980141 SPECTRUM DESIGNS PROJECTION MALAR IMPLANT
K980140 SPECTRUM DESIGNS MEDIAL MALAR IMPLANT
Search all 18 clearances from Spectrum Designs, Inc. →