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MIS Cannulated Polyaxial Reduction Screw 9.0 x 65mm

FDA UDI

Class II (US FDA UDI)

by Captiva Spine

Identity

Trade Name
MIS Cannulated Polyaxial Reduction Screw 9.0 x 65mm FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Model / Reference
16133-9065 FDA UDI

Identifiers

Primary DI / UDI-DI
M739161339065 FDA UDI
FDA Product Code
MNI FDA UDI
MNH FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone-screw internal spinal fixation system, non-sterile

MIS Cannulated Polyaxial Reduction Screw 9.0 x 65mm by Captiva Spine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Captiva Spine

Sources (1)

  • FDA UDI 3c6cda36-1792-4948-896b-89621b225e9b 32 fields · synced May 31, 2026