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

SIESTA MEDICAL, INC., PRELUDE TONGUE SUSPENSION SYSTEM

K Number: K101060 · Decision Jul 8, 2010
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
9
Applicant Total
10
Review Days
84

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Basic Information

Device Name
SIESTA MEDICAL, INC., PRELUDE TONGUE SUSPENSION SYSTEM
K Number
K101060
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5570
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siesta Medical, Inc.
Date Received
April 15, 2010
Decision Date
July 8, 2010
Product Code
ORY
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
ORY Tongue Suspension System

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Other Clearances by Siesta Medical, Inc.

K Number Device Name
K213159 Encore System
K201238 Encore System
K183310 Encore System
K133680 ENCORE SYSTEM
K121440 ENCORE TONGUE SUSPENSION SYSTEM ENCORE REMOVAL-TITRATION KIT
K121814 ENCORE TONGUE SUSPENSION SYSTEM
K111179 ENCORE TONGUE SUSPENSION SYSTEM (MONOFILAMENT #1 SUSPENSION SUTURE), ENCORE TONGUE SUSPENSION SYSTEM SYSTEM (MONOFILAMEN
K110127 PRELUDE III TONGUE SUSPENSION SYSTEM
K103179 PRELUDE II TOUNGE SUSPENSION SYSTEM