510(k) Report

FDA applicant

Nashville Surgical Instruments

Springfield, TN2 decisions1997–20080 recalls

FDA records 2 decisions for Nashville Surgical Instruments (Springfield, TN) from 1997 to 2008: 2 510(k) clearances. Most are in product codes GAR (Suture, Nonabsorbable, Synthetic, Polyamide) and GBZ (Catheter, Cholangiography). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Nashville Surgical Instruments’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2008: 1
2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nashville Surgical Instruments by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • GARSuture, Nonabsorbable, Synthetic, Polyamide1decision
  • GBZCatheter, Cholangiography1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K081366Kumar T-Anchors Hernia SetNashville Surgical Instruments · 20081cites it

What has FDA decided for it lately?

  • K081366Kumar T-Anchors Hernia SetNashville Surgical Instruments · 2008
  • K973621Pre-View Cholangiography ClampNashville Surgical Instruments · 1997

All 2 as Nashville Surgical Instruments →