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Tenodesis Screw System

FDA UDI

Class II (US FDA UDI)

by Paragon 28

Identity

Trade Name
Tenodesis Screw System FDA UDI
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name
Grappler PEEK Interference Screw 5 x 15mm FDA UDI
Model / Reference
P41-050-1500-S FDA UDI
Description
Grappler PEEK Interference Screw 5 x 15mm FDA UDI

Identifiers

Catalog Number
P41-050-1500-S FDA UDI
Primary DI / UDI-DI
00889795053756 FDA UDI
FDA Product Code
MBI FDA UDI
GMDN Term
Tendon/ligament bone anchor, non-bioabsorbable 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

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
MRI Safety
MR Unsafe FDA UDI

Category: Tendon/ligament bone anchor, non-bioabsorbable

Tenodesis Screw System by Paragon 28 — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament bone anchor, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI 89a0dbb3-3d67-4150-ba5c-c0b18a9de4d9 34 fields · synced May 30, 2026