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Spinal System 133M1360

by Biomet Spine LLC

Spinal System 133M1360 is a Class I device made by Biomet Spine LLC, listed in FDA GUDID since 25 Sep 2018 (UDI-DI 00880304837508), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00880304837508 UDI-DI Date25 Sep 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  • Withdrawn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
Spinal System
Generic name
Bone curette, reusable
Model / Ref / Catalog
133M1360
Primary DI / UDI-DI
00880304837508
FDA product code
HTF
GMDN term
Bone curette, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone curette, reusable

Other devices from Biomet Spine LLC

See all devices from Biomet Spine LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)