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MAGEC® Manual Distractor MMD-001-C

by Nuvasive Specialized Orthopedics, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00812258022242 UDI-DI Date15 Oct 2015ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
MAGEC® Manual Distractor
Generic Name
Trans-facet-screw internal spinal fixation system, sterile
Model / Ref / Catalog
MMD-001-C
Primary DI / UDI-DI
00812258022242
FDA Product Code
PGN
GMDN Term
Trans-facet-screw internal spinal fixation system, sterile
Device Class
Class II
Regulation Number
888.3070
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Trans-facet-screw internal spinal fixation system, sterile

Other devices from Nuvasive Specialized Orthopedics, Inc.

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Properties

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

Other properties (8)

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