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M.U.S.T. MINI Posterior Cervical Screws

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
M.U.S.T. MINI Posterior Cervical Screws FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
MUST MINI Polyaxial Screw 4.5 x 22 Full thread + nut FDA UDI
Model / Reference
03.75.306 FDA UDI
Description
MUST MINI Polyaxial Screw 4.5 x 22 Full thread + nut FDA UDI

Identifiers

Primary DI / UDI-DI
07630971258648 FDA UDI
510(k) Number
K200130 FDA UDI
FDA Product Code
NKG FDA UDI
KWP FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3075 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. MINI Posterior Cervical 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 abb5a237-13c0-4103-97ad-9fcb21927ac5 34 fields · synced May 30, 2026