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Juggerstitch™ 110025571

by Biomet Orthopedics, Inc.

Juggerstitch™ 110025571 is a Class II device made by Biomet Orthopedics, Inc., cleared under FDA 510(k) K150424 on 15 May 2015 and listed in FDA GUDID since 16 Mar 2017 (UDI-DI 00880304806825), 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) K150424

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 Number00880304806825 UDI-DI Date16 Mar 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK150424 Date15 May 2015DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K150424 decided 15 May 2015 Active
  • FDA GUDID UDI-DI 00880304806825 listed 16 Mar 2017 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K150424
  2. Listed FDA GUDID 00880304806825

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Juggerstitch™
Generic name
Soft-tissue/mesh anchor, non-bioabsorbable
Model / Ref / Catalog
110025571
Primary DI / UDI-DI
00880304806825
510(k) Number
FDA product code
MBI
GMDN term
Soft-tissue/mesh anchor, non-bioabsorbable
Device class
Class II
Regulation number
888.3040
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Soft-tissue/mesh anchor, non-bioabsorbable.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)