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

SILIMED SILICONE CARVING BLOCK

K Number: K981851 · Decision Jul 9, 1998
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
44
Applicant Total
9
Review Days
44

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Basic Information

Device Name
SILIMED SILICONE CARVING BLOCK
K Number
K981851
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Silimed, LLC
Date Received
May 26, 1998
Decision Date
July 9, 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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MIB), ordered by most recent decision date.

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Other Clearances by Silimed, LLC

K Number Device Name
K974479 SILIMED VAGINAL STENT
K981852 SILIMED TISSUE EXPANDER
K981835 SILIMED MALAR IMPLANT
K981850 SILIMED CHIN IMPLANTS
K981833 SILIMED NASAL L SHAPED IMPLANT
K980221 SILIMED NASAL RETAINER
K974482 SILIMED GLUTEAL IMPLANT
K974480 SILIMED CALF IMPLANT