Skip to content

Spinal System 131M1213

by Biomet Spine LLC

Spinal System 131M1213 is a Class I device made by Biomet Spine LLC, listed in FDA GUDID since 25 Sep 2018 (UDI-DI 00880304836891), 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 Number00880304836891 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  • Withdrawn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
Chisel/osteotome blade handle
Model / Ref / Catalog
131M1213
Primary DI / UDI-DI
00880304836891
FDA product code
GFI
GMDN term
Chisel/osteotome blade handle
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Chisel/osteotome blade handle

Similar devices in this category

Other devices filed under Chisel/osteotome blade handle.

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)