← Back to catalogue

JAWS Nitinol Staple System

FDA UDI

Class II (US FDA UDI)

by Paragon 28

Identity

Trade Name
JAWS Nitinol Staple System FDA UDI
Generic Name
Orthopaedic bone staple, non-adjustable FDA UDI
Device Name
Straight Staple Assembly, 8 x 8mm FDA UDI
Model / Reference
P71-008-0808-S FDA UDI
Description
Straight Staple Assembly, 8 x 8mm FDA UDI

Identifiers

Catalog Number
P71-008-0808-S FDA UDI
Primary DI / UDI-DI
00889795023650 FDA UDI
510(k) Number
K170923 FDA UDI
FDA Product Code
JDR FDA UDI
GMDN Term
Orthopaedic bone staple, non-adjustable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

Yes

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 Conditional FDA UDI

Category: Orthopaedic bone staple, non-adjustable

JAWS Nitinol Staple System by Paragon 28 — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone staple, non-adjustable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI bfe746a0-2a78-40a9-b65f-4f8aaf872909 35 fields · synced May 30, 2026