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Helical Ridge

FDA UDI

Class II (US FDA UDI)

by Medshape, Inc.

Identity

Trade Name
Helical Ridge FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Device Name
4.75MM X 15MM PEEK Interference Screw FDA UDI
Model / Reference
1400-15-0475 FDA UDI
Description
4.75MM X 15MM PEEK Interference Screw FDA UDI

Identifiers

Primary DI / UDI-DI
M97014001504750 FDA UDI
510(k) Number
K141290 FDA UDI
FDA Product Code
MBI FDA UDI
HWC FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

Helical Ridge by Medshape, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw, non-bioabsorbable, sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medshape, Inc.

Sources (1)

  • FDA UDI 288365d7-6851-4152-8da1-7bcb315b9afd 34 fields · synced May 30, 2026