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Juggerknot 110025822

by Biomet Orthopedics, Inc.

Juggerknot 110025822 is a Class II device made by Biomet Orthopedics, Inc., cleared under FDA 510(k) K150768 on 4 Sep 2015 and listed in FDA GUDID since 5 Apr 2016 (UDI-DI 00880304700741), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K150768

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00880304700741 UDI-DI Date5 Apr 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK150768 Date4 Sep 2015DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K150768 decided 4 Sep 2015 Active
  • FDA GUDID UDI-DI 00880304700741 listed 5 Apr 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K150768
  2. Listed FDA GUDID 00880304700741

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Juggerknot
Generic name
Ligament bone anchor
Model / Ref / Catalog
110025822
Primary DI / UDI-DI
00880304700741
510(k) Number
FDA product code
MBI
GMDN term
Ligament bone anchor
Device class
Class II
Regulation number
888.3040
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Related devices

Category: Ligament bone anchor

Cleared under the same submission (K150768)

and 8 more cleared under K150768

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)