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Mc+ MC907R

by Ldr Spine USA

Mc+ MC907R is a tendon/ligament graft preparation station (FDA Class II; FDA product code NKB, Thoracolumbosacral Pedicle Screw System) made by Ldr Spine USA, listed in FDA GUDID since 12 Dec 2018 (UDI-DI 03662663043588), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03662663043588 UDI-DI Date12 Dec 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Mc+
Generic name
Tendon/ligament graft preparation station
Model / Ref / Catalog
MC907R
Primary DI / UDI-DI
03662663043588
FDA product code
NKB
GMDN term
Tendon/ligament graft preparation station
Device class
Class II
Regulation number
888.3070
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Tendon/ligament graft preparation station

Similar devices in this category

Other devices filed under Tendon/ligament graft preparation station.

Other devices from Ldr Spine USA

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)