Atlas FDA

Trocar Knife

FDA premarket approval P870076/S024 · decided 2020-02-12

Approval details

PMA number
P870076
Supplement
S024
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Trocar Knife
Generic name
Laparoscopic contraceptive tubal occlusion device
Applicant
Gyrus Acmi, Inc.
Date received
2020-01-13
Decision date
2020-02-12
Days to decision
30 days
Decision code
OK30
Product code
KNH
Advisory committee
Obstetrics/Gynecology
Expedited review
No
Location
Southborough, MA
Statement
Qualification of a new supplier of the Trocar Knife (part number 004556-503) to assure that it will continue to meet the previously approved specifications for this component. The Trocar Knife is currently supplied by XL Precision and was proposed to be supplied by the new supplier RMS Surgical.

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