# K014305: Resorbable Lactosorb-L Acl Crosspin

- Pathway: 510(k) (Traditional)
- Applicant: Arthrotek, Inc.
- Decided: Mar 29, 2002 after 88 days
- Product code: HTY (Pin, Fixation, Smooth)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K933948 (1994). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982497: Arthrotek Interference Screw, Biomet, Inc. (1998). Our OCR of the scanned summary read K988497, which is not a number in FDA’s lists. Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “Arthrotek Interference Screw”.
- K974341: Mitek BTB Absorbable (Pla) Cross Pin, Mitek Products (1998) Summary page 1.
- K941941: Bone Mulch Screw, Biomet, Inc. (1995) Summary page 1.
- K991298: Bone Mulch Screw System, Biomet, Inc. (1999) Summary page 1.
- K993025: Modification to Bone Mulch Screw System, Biomet, Inc. (1999) Summary page 1.
- K011172: Arthrex Bio-Transfix, Arthrex, Inc. (2001)

## Indications for use
The Resorbable LactoSorb-L® ACL Crosspin is indicated for ACL reconstruction.

Source page: https://510kreport.com/device/K014305
Methodology: https://510kreport.com/methodology