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

ACCORDION STONE MANAGEMENT DEVICE MODEL AC281205 AND AC3814510

K Number: K102887 · Decision May 16, 2011
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
51
Applicant Total
6
Review Days
228

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Basic Information

Device Name
ACCORDION STONE MANAGEMENT DEVICE MODEL AC281205 AND AC3814510
K Number
K102887
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4680
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Percutaneous Systems, Inc.
Date Received
September 30, 2010
Decision Date
May 16, 2011
Product Code
FFL
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FFL Dislodger, Stone, Basket, Ureteral, Metal

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Other Clearances by Percutaneous Systems, Inc.

K Number Device Name
K082803 COAXIAL ACCORDION STONE MANAGEMENT DEVICE, MODEL: COAC12005 - COA20015
K052134 CYSTOGLIDE DILATING INTRODUCER SHEATH
K042877 MICROVERTER URETERAL ACCESS SHEATH
K040519 SLIP UROLOGY CATHETER
K040520 SLIP UROLOGY INTRODUCER SHEATH