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Lesser Metatarsal Shortening System

FDA UDI

Class I (US FDA UDI)

by Paragon 28

Identity

Trade Name
Lesser Metatarsal Shortening System FDA UDI
Generic Name
Surgical saw blade, oscillating, single-use FDA UDI
Device Name
Saw Blade 9 x 31 x .051mm Stryker (Sterile) FDA UDI
Model / Reference
P99-151-P30S-1-S FDA UDI
Description
Saw Blade 9 x 31 x .051mm Stryker (Sterile) FDA UDI

Identifiers

Catalog Number
P99-151-P30S-1-S FDA UDI
Primary DI / UDI-DI
00889795111029 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical saw blade, oscillating, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical saw blade, oscillating, single-use

Lesser Metatarsal Shortening System by Paragon 28 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical saw blade, oscillating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI b03d5bb3-c1c3-40b9-a6db-b5bc156ef1b9 34 fields · synced May 30, 2026