NGM WAVE PLIF Cage 11 x 24 mm 12°

by NGMedical GmbH GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04251631405733 UDI-DI	Date14 Jul 2022Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name: NGM WAVE PLIF Cage
Generic Name: Polymeric spinal interbody fusion cage
Model / Ref / Catalog: 11 x 24 mm 12°, WE112412

Primary DI / UDI-DI: 04251631405733
510(k) Number: K212050
FDA Product Code: MAX
GMDN Term: Polymeric spinal interbody fusion cage

Device Class: Class II
Regulation Number: 888.3080
GUDID distribution status: In Commercial Distribution

MRI Safety: MR Unsafe

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Class IIa
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Properties

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

Other properties (7)

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