Last synced on 20 December 2024 at 11:05 pm

A.I.M. Lead Loop Suturing Device (1), A.I.M. Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (1) plus Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (2), A.I.M. Lead Loop Suturing Device plus Tension Assist/Suture Cutter Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150924
510(k) Type
Traditional
Applicant
ANCHOR INNOVATION MEDICAL (A.I.M.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/2015
Days to Decision
112 days
Submission Type
Summary

A.I.M. Lead Loop Suturing Device (1), A.I.M. Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (1) plus Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (2), A.I.M. Lead Loop Suturing Device plus Tension Assist/Suture Cutter Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150924
510(k) Type
Traditional
Applicant
ANCHOR INNOVATION MEDICAL (A.I.M.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/2015
Days to Decision
112 days
Submission Type
Summary