Pagoda 752-0101A

by Ortho Development Corp.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00822409021253 UDI-DI	Date15 Jul 2016Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Pagoda
Generic Name: Bone-screw internal spinal fixation system connector
Model / Reference: 752-0101A

Primary DI / UDI-DI: 00822409021253
510(k) Number: K131785
FDA Product Code: MNI, NKB, MNH
GMDN Term: Bone-screw internal spinal fixation system connector

Device Class: Class II
Regulation Number: 888.3070
GUDID distribution status: In Commercial Distribution

Size: Width — 25 Millimeter

Other devices from Ortho Development Corp.

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Class I
N/A 233-0138

Class I
N/A 233-0139

Class I
N/A 233-0140

Class I
N/A 233-0142

Class I
N/A 233-0141

Class I

See all devices from Ortho Development Corp. →

Properties

Sterile
Single Use
Implantable
Prescription Use
Lot / Batch Number
Expiration Date

Other properties (8)

Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Manufacturing Date: No