510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K925328Substantially Equivalent

Anspach Bone Rivet, Anspach Suture Anchor

Anspach Mfg., Inc., Lake Park FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925328 is the FDA 510(k) clearance record for ANSPACH BONE RIVET, ANSPACH SUTURE ANCHOR, a class II device, cleared for Anspach Mfg., Inc. on under FDA product code HWC (Screw, Fixation, Bone). FDA records list 3 510(k) clearances for Anspach Mfg., Inc., from to . As of , FDA records show no recalls naming K925328.

Clearance record

Decision date
Received
(371 days to decision)
Product code
HWC Screw, Fixation, Bone
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
Anspach Mfg., Inc. 1349 S. Killian Dr., Lake Park FL
510(k) summary
Summary
Third party review
No

Clearances, product code HWC

Trailing 12 months
21 clearances under product code HWC in the twelve months to October 2026, May 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code HWC, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20262
April 20263
May 20264
June 20262
July 20261
August 20263
September 20264
October 20260