510(k) · Cleared

Cleared

Adaptive Wedge

K110662510(k) TraditionalCleared Mar 12, 2012370-day reviewClass II21 CFR 888.3030

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

Adaptive Specialty, LLC · HRS Plate, Fixation, Bone

Cleared on Mar 12, 2012 as substantially equivalent to K073535 (Wrightmedicaltechnologyinc, 2008) and 1 other predicate after a 370-day review. Its family tree reaches back 1 generation to 2008.

Decided: Mar 12, 2012
Review: 370 days
Class: Class II
Product code: HRS
Recalls: None
Predicates: 2

Its longest line of descent runs back 1 generation to K073535 (2008). 2 ancestors in all. No later device cites it as a predicate yet.

By dateBy generation

Root · 1 generation backK073535 Biofoam Bone WedgeWrightmedicaltechnologyinc · 2008
This deviceK110662 Adaptive WedgeAdaptive Specialty, LLC · 2012

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K073535	Biofoam Bone Wedge	Wrightmedicaltechnologyinc	2008	—
0 (this device)	K110662	Adaptive Wedge	Adaptive Specialty, LLC	2012	—

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
2010	1	0

FIG. 1 — Lineage of K110662, 2008–2012Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 HRS? 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 HRS device

#1 K222465 Tyber Medical Anatomical Plating Systemscore 27.5 · 16 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

Get a 510(k) Report

What was it cleared against? (2)

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.

Type	Number	Device	Applicant	Decided	Recalls
*	K073535	Biofoam Bone Wedge Summary page 1 …HIRS Class HI 3. Predicate or legally marketed devices which are substantially equivalent: BIOFOAM Tm Bone Wedge (K073535 / K093950) 4. Description of the device: The Adaptive Wedge has a distinct design to help facilitate bony integration once…	Wrightmedicaltechnologyinc	2008	—
*	K093950	Biofoam Bone Wedge Model Assorted Summary page 1 …HIRS Class HI 3. Predicate or legally marketed devices which are substantially equivalent: BIOFOAM Tm Bone Wedge (K073535 / K093950) 4. Description of the device: The Adaptive Wedge has a distinct design to help facilitate bony integration once implanted,…	Wrightmedicaltechnologyinc	2010	—

Also cleared against K073535: 3 other devices →

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?

None of the 2 ancestors has a recall.
3 other devices also cite its predicate K073535.

How does its category compare?

All HRS devices

HRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · HRS

54in 2025

2007high 76 (2014) · low 35 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HRS

90in 2025

2007high 144 (2022) · low 57 (2014)2026

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

Recalls per year · HRS

1in 2025

2007high 25 (2019) · low 0 (2014)2026

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

Adverse event reports per year · HRS

2,306in 2025

2007high 3,359 (2019) · low 311 (2008)2025

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

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	35	63	2	339
2008	35	87	11	311
2009	47	85	3	435
2010	49	100	16	491
2011	43	88	5	773
2012	59	106	4	1,663
2013	56	89	11	2,643
2014	76	57	0	2,413
2015	56	97	7	3,095
2016	44	109	5	2,276
2017	57	122	3	2,220
2018	40	116	2	2,663
2019	46	89	25	3,359
2020	48	88	1	2,790
2021	40	87	9	2,442
2022	47	144	3	1,700
2023	40	120	1	2,049
2024	54	96	0	1,849
2025	54	90	1	2,306
2026	51	82	3	—

What is it indicated for?

The Adaptive Wedge is intended to be used for internal bone fixation for small bone fractures or osteotomies in the ankle and foot such as:

Opening wedge osteotomies of Hallux Valgus

Evans lengthening osteotomnies

Cotton osteotomy

This device is intended for use with ancillary fixation and is not intended for use in the spine.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K110662 · printed Nov 6, 2026

Cite this page

510(k) Report. “K110662: Adaptive Wedge.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110662

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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