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2.0mm System 01-7607

by Biomet Microfixation, Inc

2.0mm System 01-7607 is a Class II device made by Biomet Microfixation, Inc, cleared under FDA 510(k) K121624 on 12 Oct 2012 (2 earlier submissions) and listed in FDA GUDID since 11 Oct 2015 (UDI-DI 00841036014650), active as of 23 Oct 2026. 3 FDA recalls are linked to it.

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

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

4 closed

Documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841036014650 UDI-DI Date11 Oct 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK121624 Date12 Oct 2012DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K121624 decided 12 Oct 2012 Active· +2 more in the status table
  • FDA GUDID UDI-DI 00841036014650 listed 11 Oct 2015 Listed

Recalls

4 recalls · FDA

    • Terminated Z-1220-2017 FDA Class II initiated 10 Jan 2017 on shared 510(k) K121589

    The identification of the devices was non-conforming with off-centered slots and the no-go gage starting in the pilot hole.

  • 2 recalls, same reason

    • Terminated Z-0137-2016 FDA Class II initiated 6 Aug 2015
    • Terminated Z-0136-2016 FDA Class II initiated 6 Aug 2015

    The lids on implant caddies within P/N 17-5000 and 19-5000 could not be opened by the user without application of undesirable/unexpected excessive force.

    • Terminated Z-0108-2011 FDA Unclassified (pre-2012) initiated 31 Aug 2010

    Mislabeled size: The 2.0/1.0 4 hole long plate, Lot 120150 is labeled as 01-9205 (2.0/1.0 4 Hole Long Plate), however, the package contains a 01-9204 (2.0/1.0 4 Hole Regular Plate).

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Timeline

8 dated events

  1. Cleared FDA 510(k) K854886
  2. Recall initiated FDA recalls Z-0108-2011
  3. Cleared FDA 510(k) K121589
  4. Cleared FDA 510(k) K121624
  5. Recall initiated FDA recalls Z-0137-2016
  6. Recall initiated FDA recalls Z-0136-2016
  7. Listed FDA GUDID 00841036014650
  8. Recall initiated FDA recalls Z-1220-2017

Coverage

1 jurisdiction

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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
"2.0mm" System
Generic name
Orthopaedic bone screw, non-bioabsorbable, non-sterile
Model / Ref / Catalog
01-7607
Primary DI / UDI-DI
00841036014650
510(k) Number
FDA product code
HBW, GXR, JEY, GWO
GMDN term
Orthopaedic bone screw, non-bioabsorbable, non-sterile
Device class
Class II
Regulation number
882.5360, 882.5250, 872.4760, 882.5320
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic bone screw, non-bioabsorbable, non-sterile

Cleared under the same submission (K121589)

and 8 more cleared under K121589

Cleared under the same submission (K121624)

and 8 more cleared under K121624

Similar devices in this category

Other devices filed under Orthopaedic bone screw, non-bioabsorbable, non-sterile.

Other devices from Biomet Microfixation, Inc

See all devices from Biomet Microfixation, Inc →

Properties

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