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

Signia™ Circular Adapter (Standard Length) (SIGCIRSTND); Signia™ Circular Adapter XL Length (SIGCIRXL)

K Number: K240881 · Decision Nov 1, 2024
Classifications
1
FEI Numbers
76
Registration Numbers
76
Same Product Code
41
Applicant Total
2
Review Days
214

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Basic Information

Device Name
Signia™ Circular Adapter (Standard Length) (SIGCIRSTND); Signia™ Circular Adapter XL Length (SIGCIRXL)
K Number
K240881
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Covidien (Part of Medtronic)
Date Received
April 1, 2024
Decision Date
November 1, 2024
Product Code
GAG
Advisory Committee
General Hospital
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
GAG Stapler, Surgical

Similar 510(k) Clearances

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

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Other Clearances by Covidien (Part of Medtronic)

K Number Device Name
K253657 Tri-staple 2.0™ Reloads; Endo GIA™ Reloads with Tri-Staple™ Technology; Endo GIA™ Gray Articulating Reloads; Signia™ Small Diameter Reloads