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

OverStitch SX Endoscopic Suturing System (ESS)

K Number: K171886 · Decision Nov 15, 2017
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
69
Applicant Total
12
Review Days
142

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Basic Information

Device Name
OverStitch SX Endoscopic Suturing System (ESS)
K Number
K171886
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Apollo Endosurgery, Inc.
Date Received
June 26, 2017
Decision Date
November 15, 2017
Product Code
OCW
Advisory Committee
Gastroenterology, Urology
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
OCW Endoscopic Tissue Approximation Device

Similar 510(k) Clearances

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

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Other Clearances by Apollo Endosurgery, Inc.

K Number Device Name
K232544 Apollo ESG NXT System, Apollo REVISE NXT System
K231553 OverStitch NXT Endoscopic Suturing System
DEN210045 APOLLO ESG System, APOLLO ESG SX System, APOLLO REVISE System, APOLLO REVISE SX System
K210266 OverStitch Sx Endoscopic Suturing System
K201808 X-Tack Endoscopic HeliX Tacking System
K122270 OVERTUBE ENDOSCOPIC ACCESS SYSTEM
K103155 SUMO ACCESS AND TISSUE RESECTION SYSTEM
K082102 GASTRIC PORT, MODELS: GAP-0016-00, GAP-0018-00, GAP-0020-00
K090583 ENDOSCOPIC MONOPOLAR SCISSORS, MODELS EMS-235, EMS-165
K082114 ELECTROCAUTERY DILATION BALLOON, MODELS: EDB-0018-00, EDB-0020-00, EDB-0022-00
Search all 12 clearances from Apollo Endosurgery, Inc. →