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Devices
Device Recall PopLok Punch
Model / Serial
Lot 318455
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution -- US and Korea.
Product Description
PopLok Punch labeled in part: || "PKL-35M***3.5mm***QTY 1***PopLok Punch***ConMed Linvatec Biomaterials, Ltd. Hermiankatu 6-8L 33720 Tampere, FINLAND***Rx Only***ConMed Linvatec 11311 Concept Blvd Largo, FL 33773-4908 USA***Made in USA***" || Intended Use: Bone Punch.
Manufacturer
Linvatec Corp. dba ConMed Linvatec
1 Event
Recall of Device Recall PopLok Punch
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Manufacturer
Linvatec Corp. dba ConMed Linvatec
Manufacturer Address
Linvatec Corp. dba ConMed Linvatec, 11311 Concept Blvd, Largo FL 33773-4908
Manufacturer Parent Company (2017)
CONMED Corp.
Source
USFDA
One device with a similar name
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Device Recall PopLok Punch 3.5MM
Model / Serial
Lot 256058
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution - USA including California and Internationally to Spain and Korea
Product Description
ConMed Linvatec Biomaterials, PopLok bone Punch PKL-35M, 3.5mm || Orthopedic manual surgical instrument - Bone Punch
Manufacturer
Linvatec Corp. dba ConMed Linvatec
Language
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