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Manufacturers
NuVasive Inc
Manufacturer Address
NuVasive Inc, 7475 Lusk Blvd, San Diego CA 92121-5707
Manufacturer Parent Company (2017)
NuVasive, Inc.
Source
USFDA
31 Events
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
Recall of Device Recall SpheRx Posted Pedicle Screw System
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31 devices in the database
Device Recall SpheRx Posted Pedicle Screw System
Model / Serial
Batch: JK2082, JK2095, JK2165
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.
Product Description
5.5mm x 50mm Cannulated Screw Shank || Subsequent Codes: KWP, KWQ, MNH, MNI
Device Recall SpheRx Posted Pedicle Screw System
Model / Serial
Batch: JK2059, JK2084, JK2148
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.
Product Description
5.5mm x 55mm Cannulated Screw Shank || Subsequent Codes: KWP, KWQ, MNH, MNI
Device Recall SpheRx Posted Pedicle Screw System
Model / Serial
Batch: JK2057, JK2157.
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.
Product Description
6.5mm x 30mm Cannulated Screw Shank || Subsequent Codes: KWP, KWQ, MNH, MNI
Device Recall SpheRx Posted Pedicle Screw System
Model / Serial
Batch: JK2083, JK2184
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.
Product Description
6.5mm x 35mm Cannulated Screw Shank || Subsequent Codes: KWP, KWQ, MNH, MNI
Device Recall SpheRx Posted Pedicle Screw System
Model / Serial
Batch: JK2039, JK2072, JK2168.
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.
Product Description
6.5mm x 50mm Cannulated Screw Shank || Subsequent Codes: KWP, KWQ, MNH, MNI
26 more
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