Pagoda

FDA UDI

Class II (US FDA UDI)

by Ortho Development Corp.

Identity

Trade Name: Pagoda FDA UDI
Generic Name: Bone-screw internal spinal fixation system rod FDA UDI
Device Name: Diameter 5.5 mm x 80 mm Curved Rod One Stripe Ti FDA UDI
Model / Reference: 158-0080-01A FDA UDI
Description: Diameter 5.5 mm x 80 mm Curved Rod One Stripe Ti FDA UDI

Identifiers

Primary DI / UDI-DI: 00822409019199 FDA UDI
510(k) Number: K131785 FDA UDI
FDA Product Code: MNH FDA UDI
NKB FDA UDI
MNI FDA UDI
GMDN Term: Bone-screw internal spinal fixation system rod FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3070 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 80 Millimeter FDA UDI
Outer Diameter — 5.5 Millimeter FDA UDI

Category: Bone-screw internal spinal fixation system rod

Pagoda by Ortho Development Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system rod.

The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd. · Class II
LnK Spinal Fixation System — L&K BIOMED CO. , LTD. · Class II
Whistler Modular Pedicle Screw System — EVOLUTION SPINE, LLC · Class II
Proficient® Posterior Cervical Spine System — Spine Wave, Inc. · Class II
Proficient™ Posterior Cervical Spine System — Spine Wave, Inc. · Class II
The JASPER Spinal Fixation System60 — GBS Commonwealth Co., Ltd. · Class II
The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd. · Class II
Fortex Pedicle Screw System — Xtant Medical Holdings, Inc. · Class II

Cleared under the same submission

K131785 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Ortho Development Corp.

Sources (1)

FDA UDI 6002300f-3abf-4aa6-9d3e-1e0c0642c415 36 fields · synced Jun 8, 2026