510(k) Report

510(k) · Cleared

Cleared

DORO Sterile Disposable Skull Pins Stainless Steel, Adult (36 pcs) (3006-00); DORO Sterile Disposable Skull Pins Stainless Steel, Pediatric (36 pcs) (3006-10); DORO Sterile Disposable Skull Pin Titanium, Adult (36 pcs) (3006-20); DORO Sterile Disposable Skull Pin Titanium, Pediatric (36 pcs) (3006-30); DORO Sterile Disposable Skull Pin Stainless Steel, Adult (36 pcs) (3006-50)

K241883510(k) SpecialCleared Jul 26, 202428-day reviewClass II21 CFR 882.4460

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Pro Med Instruments GmbH · HBL Holder, Head, Neurosurgical (Skull Clamp)

Cleared on Jul 26, 2024 as substantially equivalent to K193438 (Pro Med Instruments GmbH, 2020) after a 28-day review. Its family tree reaches back 3 generations to 1993.

Decided
Jul 26, 2024
Review
28 days
Class
Class II
Product code
HBL
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K923789 (1993). 6 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 3 generations backK923789 Mayfield Adult Disposable Skull PinOhio Medical Instrument Co., Inc. · 1993
  2. 2 generations backK073163 Limited Artifact Skull Pin, Model 0107Dinkler Surgical Devices, Inc. · 2008
  3. 1 generation backK193438 DORO Sterile Disposable Skull Pins (Stainless Steel) , DORO Sterile…Pro Med Instruments GmbH · 2020
  4. This deviceK241883 DORO Sterile Disposable Skull Pins Stainless Steel, Adult (36 pcs)…Pro Med Instruments GmbH · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K923789Mayfield Adult Disposable Skull PinOhio Medical Instrument Co., Inc.1993—
−2K073163Limited Artifact Skull Pin, Model 0107Dinkler Surgical Devices, Inc.2008—
−1K193438DORO Sterile Disposable Skull Pins (Stainless Steel) , DORO Sterile Disposable…Pro Med Instruments GmbH2020—
0 (this device)K241883DORO Sterile Disposable Skull Pins Stainless Steel, Adult (36 pcs) (3006-00)…Pro Med Instruments GmbH2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199510
201710
FIG. 1 — Lineage of K241883, 1993–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in HBL? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new HBL device

  1. #1 K250423 mb-FIX Cranial Stabilization Systemsscore 13.0 · 10 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K193438DORO Sterile Disposable Skull Pins (Stainless Steel) , DORO Sterile Disposable Skull…
Summary page 6
…l Pins (Stainless Steel) DORO® Sterile Model: K193438 pro med instruments GmbH Disposable Skull Pins 3006-00 Stainless Steel, Adu…
Pro Med Instruments GmbH2020—

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 31 years and passes through 3 companies; a new generation was cleared every 12.3 years on median.
  • None of the 6 ancestors has a recall.

How does its category compare?

All HBL devices

HBL Holder, Head, Neurosurgical (Skull Clamp): FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · HBL

1in 2025

2007: 32008: 22009: 32010: 12011: 12012: 22013: 22014: 22017: 12019: 22020: 22021: 12024: 22025: 1
2007high 3 (2007) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HBL

54in 2009

2007: 30 days median2009: 54 days median
2007high 54 (2009) · low 30 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · HBL

1in 2025

2012: 12013: 12017: 12019: 12020: 12022: 12025: 1
2007high 1 (2012) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · HBL

272in 2025

2007: 392008: 1032009: 972010: 1542011: 1992012: 1702013: 1482014: 1662015: 1962016: 2802017: 2962018: 3052019: 1,0282020: 6072021: 5122022: 2682023: 2652024: 1972025: 272
2007high 1,028 (2019) · low 39 (2007)2025

MAUDE reports naming product code HBL, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007330039
20082—0103
2009354097
20101—0154
20111—0199
20122—1170
20132—1148
20142—0166
20150—0196
20160—0280
20171—1296
20180—0305
20192—11,028
20202—1607
20211—0512
20220—1268
20230—0265
20242—0197
20251—1272
20260—0—

What is it indicated for?

Indicated for use in combination with a skull clamp in open and percutaneous craniotomies as well as spinal surgery when rigid fixation is necessary.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K241883: DORO Sterile Disposable Skull Pins Stainless Steel, Adult (36 pcs) (3006-00); DORO Sterile Disposable Skull Pins Stainless Steel, Pediatric (36 pcs) (3006-10); DORO Sterile Disposable Skull Pin Titanium, Adult (36 pcs) (3006-20); DORO Sterile Disposable Skull Pin Titanium, Pediatric (36 pcs) (3006-30); DORO Sterile Disposable Skull Pin Stainless Steel, Adult (36 pcs) (3006-50).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K241883

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026