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M.U.S.T. Polyaxial Pedicle Screw

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
M.U.S.T. Polyaxial Pedicle Screw FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Enh. Pedicle Screw 4.5x30mm + Nut (1x) - Sterile FDA UDI
Model / Reference
03.50.303 FDA UDI
Description
Enh. Pedicle Screw 4.5x30mm + Nut (1x) - Sterile FDA UDI

Identifiers

Primary DI / UDI-DI
07630030856792 FDA UDI
510(k) Number
K141988 FDA UDI
FDA Product Code
KWQ FDA UDI
KWP FDA UDI
NKB FDA UDI
MNH FDA UDI
MNI FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
888.3050 FDA UDI
888.3070 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Spinal bone screw, non-bioabsorbable

M.U.S.T. Polyaxial Pedicle Screw by Medacta International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 67b99f1f-43e1-47a4-a43c-86da46214a25 34 fields · synced May 30, 2026