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M.U.S.T. Reduction Pedicle Screws

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
M.U.S.T. Reduction Pedicle Screws FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Reduction Pedicle Screw 5x35 mm FDA UDI
Model / Reference
03.50.710 FDA UDI
Description
Reduction Pedicle Screw 5x35 mm FDA UDI

Identifiers

Primary DI / UDI-DI
07630030846809 FDA UDI
510(k) Number
K153664 FDA UDI
FDA Product Code
NKB FDA UDI
MNI FDA UDI
MNH FDA UDI
KWQ FDA UDI
KWP FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3060 FDA UDI
888.3050 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. Reduction Pedicle Screws 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 e42327c8-99dd-4e88-894a-1a56f699df2a 34 fields · synced May 30, 2026